Canonical Allele Identifier: CA658823977
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 548173
ClinVar RCV Id: RCV000660940
dbSNP Id: rs1555588074

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092273_43092274insTC , CM000679.2:g.43092273_43092274insTC GRCh38
NC_000017.10:g.41244290_41244291insTC , CM000679.1:g.41244290_41244291insTC GRCh37
NC_000017.9:g.38497816_38497817insTC NCBI36
NG_005905.2:g.125710_125711insGA , LRG_292:g.125710_125711insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3321_3322insGA
ENST00000461574.2:c.3257_3258insGA ENSP00000417241.2:p.Gly1087LysfsTer23
ENST00000470026.6:c.3257_3258insGA ENSP00000419274.2:p.Gly1087LysfsTer23
ENST00000473961.6:c.3131_3132insGA ENSP00000420201.2:p.Gly1045LysfsTer23
ENST00000476777.6:c.3254_3255insGA ENSP00000417554.2:p.Gly1086LysfsTer23
ENST00000477152.6:c.3179_3180insGA ENSP00000419988.2:p.Gly1061LysfsTer23
ENST00000478531.6:c.785-1242_785-1241insGA ENSP00000420412.2:n.785-1242_785-1241insGA
ENST00000489037.2:c.3179_3180insGA ENSP00000420781.2:p.Gly1061LysfsTer23
ENST00000493919.6:c.647-1242_647-1241insGA ENSP00000418819.2:n.647-1242_647-1241insGA
ENST00000494123.6:c.3257_3258insGA ENSP00000419103.2:p.Gly1087LysfsTer23
ENST00000497488.2:c.2369_2370insGA ENSP00000418986.2:p.Gly791LysfsTer23
ENST00000618469.2:c.3257_3258insGA ENSP00000478114.2:p.Gly1087LysfsTer23
ENST00000634433.2:c.3134_3135insGA ENSP00000489431.2:p.Gly1046LysfsTer23
ENST00000644379.2:c.3257_3258insGA ENSP00000496570.2:p.Gly1087LysfsTer23
ENST00000644555.2:c.647-1242_647-1241insGA ENSP00000494614.2:n.647-1242_647-1241insGA
ENST00000652672.2:c.3116_3117insGA ENSP00000498906.2:p.Gly1040LysfsTer23
ENST00000484087.6:c.665-1242_665-1241insGA ENSP00000419481.2:n.665-1242_665-1241insGA
ENST00000700182.1:c.707-1242_707-1241insGA ENSP00000514849.1:n.707-1242_707-1241insGA
ENST00000357654.9:c.3257_3258insGA MANE Select ENSP00000350283.3:p.Gly1087LysfsTer23
ENST00000471181.7:c.3257_3258insGA ENSP00000418960.2:p.Gly1087LysfsTer23
ENST00000352993.7:c.671-1242_671-1241insGA ENSP00000312236.5:n.671-1242_671-1241insGA
ENST00000354071.7:c.3257_3258insGA ENSP00000326002.7:p.Gly1087LysfsTer23
ENST00000357654.7:c.3257_3258insGA ENSP00000350283.3:p.Gly1087LysfsTer23
ENST00000461221.5:c.*3040_*3041insGA ENSP00000418548.1:n.*3040_*3041insGA
ENST00000468300.5:c.788-1242_788-1241insGA ENSP00000417148.1:n.788-1242_788-1241insGA
ENST00000471181.6:c.3257_3258insGA ENSP00000418960.2:p.Gly1087LysfsTer23
ENST00000478531.5:c.785-1242_785-1241insGA ENSP00000420412.1:n.785-1242_785-1241insGA
ENST00000484087.5:c.410-1242_410-1241insGA ENSP00000419481.1:n.410-1242_410-1241insGA
ENST00000487825.5:c.413-1242_413-1241insGA ENSP00000418212.1:n.413-1242_413-1241insGA
ENST00000491747.6:c.788-1242_788-1241insGA ENSP00000420705.2:n.788-1242_788-1241insGA
ENST00000493795.5:c.3116_3117insGA ENSP00000418775.1:p.Gly1040LysfsTer23
ENST00000493919.5:c.647-1242_647-1241insGA ENSP00000418819.1:n.647-1242_647-1241insGA
ENST00000586385.5:c.5-28323_5-28322insGA ENSP00000465818.1:n.5-28323_5-28322insGA
ENST00000591534.5:c.-43-17753_-43-17752insGA ENSP00000467329.1:n.-43-17753_-43-17752insGA
ENST00000591849.5:c.-99+32997_-99+32998insGA ENSP00000465347.1:n.-99+32997_-99+32998insGA
NM_007294.3:c.3257_3258insGA , LRG_292t1:c.3257_3258insGA NP_009225.1:p.Gly1087LysfsTer23
NM_007297.3:c.3116_3117insGA NP_009228.2:p.Gly1040LysfsTer23
NM_007298.3:c.788-1242_788-1241insGA NP_009229.2:n.788-1242_788-1241insGA
NM_007299.3:c.788-1242_788-1241insGA NP_009230.2:n.788-1242_788-1241insGA
NM_007300.3:c.3257_3258insGA NP_009231.2:p.Gly1087LysfsTer23
NR_027676.1:n.3393_3394insGA
NM_007294.4:c.3257_3258insGA MANE Select NP_009225.1:p.Gly1087LysfsTer23
NM_007297.4:c.3116_3117insGA NP_009228.2:p.Gly1040LysfsTer23
NM_007299.4:c.788-1242_788-1241insGA NP_009230.2:n.788-1242_788-1241insGA
NM_007300.4:c.3257_3258insGA NP_009231.2:p.Gly1087LysfsTer23
NR_027676.2:n.3434_3435insGA