Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092507_43092511delinsCATTG , CM000679.2:g.43092507_43092511delinsCATTG	GRCh38
NC_000017.10:g.41244524_41244528delinsCATTG , CM000679.1:g.41244524_41244528delinsCATTG	GRCh37
NC_000017.9:g.38498050_38498054delinsCATTG	NCBI36
NG_005905.2:g.125473_125477delinsCAATG , LRG_292:g.125473_125477delinsCAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3084_3088delinsCAATG
ENST00000461574.2:c.3020_3024delinsCAATG	ENSP00000417241.2:p.Ser1007=
ENST00000470026.6:c.3020_3024delinsCAATG	ENSP00000419274.2:p.Ser1007=
ENST00000473961.6:c.2894_2898delinsCAATG	ENSP00000420201.2:p.Ser965=
ENST00000476777.6:c.3017_3021delinsCAATG	ENSP00000417554.2:p.Ser1006=
ENST00000477152.6:c.2942_2946delinsCAATG	ENSP00000419988.2:p.Ser981=
ENST00000478531.6:c.785-1479_785-1475delinsCAATG	ENSP00000420412.2:n.785-1479_785-1475delinsCAATG
ENST00000489037.2:c.2942_2946delinsCAATG	ENSP00000420781.2:p.Ser981=
ENST00000493919.6:c.647-1479_647-1475delinsCAATG	ENSP00000418819.2:n.647-1479_647-1475delinsCAATG
ENST00000494123.6:c.3020_3024delinsCAATG	ENSP00000419103.2:p.Ser1007=
ENST00000497488.2:c.2132_2136delinsCAATG	ENSP00000418986.2:p.Ser711=
ENST00000618469.2:c.3020_3024delinsCAATG	ENSP00000478114.2:p.Ser1007=
ENST00000634433.2:c.2897_2901delinsCAATG	ENSP00000489431.2:p.Ser966=
ENST00000644379.2:c.3020_3024delinsCAATG	ENSP00000496570.2:p.Ser1007=
ENST00000644555.2:c.647-1479_647-1475delinsCAATG	ENSP00000494614.2:n.647-1479_647-1475delinsCAATG
ENST00000652672.2:c.2879_2883delinsCAATG	ENSP00000498906.2:p.Ser960=
ENST00000484087.6:c.665-1479_665-1475delinsCAATG	ENSP00000419481.2:n.665-1479_665-1475delinsCAATG
ENST00000700182.1:c.707-1479_707-1475delinsCAATG	ENSP00000514849.1:n.707-1479_707-1475delinsCAATG
ENST00000357654.9:c.3020_3024delinsCAATG MANE Select	ENSP00000350283.3:p.Ser1007=
ENST00000471181.7:c.3020_3024delinsCAATG	ENSP00000418960.2:p.Ser1007=
ENST00000352993.7:c.671-1479_671-1475delinsCAATG	ENSP00000312236.5:n.671-1479_671-1475delinsCAATG
ENST00000354071.7:c.3020_3024delinsCAATG	ENSP00000326002.7:p.Ser1007=
ENST00000357654.7:c.3020_3024delinsCAATG	ENSP00000350283.3:p.Ser1007=
ENST00000461221.5:c.2803_2807delinsCAATG	ENSP00000418548.1:n.2803_2807delinsCAATG
ENST00000468300.5:c.788-1479_788-1475delinsCAATG	ENSP00000417148.1:n.788-1479_788-1475delinsCAATG
ENST00000471181.6:c.3020_3024delinsCAATG	ENSP00000418960.2:p.Ser1007=
ENST00000478531.5:c.785-1479_785-1475delinsCAATG	ENSP00000420412.1:n.785-1479_785-1475delinsCAATG
ENST00000484087.5:c.410-1479_410-1475delinsCAATG	ENSP00000419481.1:n.410-1479_410-1475delinsCAATG
ENST00000487825.5:c.413-1479_413-1475delinsCAATG	ENSP00000418212.1:n.413-1479_413-1475delinsCAATG
ENST00000491747.6:c.788-1479_788-1475delinsCAATG	ENSP00000420705.2:n.788-1479_788-1475delinsCAATG
ENST00000493795.5:c.2879_2883delinsCAATG	ENSP00000418775.1:p.Ser960=
ENST00000493919.5:c.647-1479_647-1475delinsCAATG	ENSP00000418819.1:n.647-1479_647-1475delinsCAATG
ENST00000586385.5:c.5-28560_5-28556delinsCAATG	ENSP00000465818.1:n.5-28560_5-28556delinsCAATG
ENST00000591534.5:c.-43-17990_-43-17986delinsCAATG	ENSP00000467329.1:n.-43-17990_-43-17986delinsCAATG
ENST00000591849.5:c.-99+32760_-99+32764delinsCAATG	ENSP00000465347.1:n.-99+32760_-99+32764delinsCAATG
NM_007294.3:c.3020_3024delinsCAATG , LRG_292t1:c.3020_3024delinsCAATG	NP_009225.1:p.Ser1007=
NM_007297.3:c.2879_2883delinsCAATG	NP_009228.2:p.Ser960=
NM_007298.3:c.788-1479_788-1475delinsCAATG	NP_009229.2:n.788-1479_788-1475delinsCAATG
NM_007299.3:c.788-1479_788-1475delinsCAATG	NP_009230.2:n.788-1479_788-1475delinsCAATG
NM_007300.3:c.3020_3024delinsCAATG	NP_009231.2:p.Ser1007=
NR_027676.1:n.3156_3160delinsCAATG
NM_007294.4:c.3020_3024delinsCAATG MANE Select	NP_009225.1:p.Ser1007=
NM_007297.4:c.2879_2883delinsCAATG	NP_009228.2:p.Ser960=
NM_007299.4:c.788-1479_788-1475delinsCAATG	NP_009230.2:n.788-1479_788-1475delinsCAATG
NM_007300.4:c.3020_3024delinsCAATG	NP_009231.2:p.Ser1007=
NR_027676.2:n.3197_3201delinsCAATG