Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38502813_38502831delinsGAGCAGGGGCAGGGGCAGC , CM000681.2:g.38502813_38502831delinsGAGCAGGGGCAGGGGCAGC	GRCh38
NC_000019.9:g.38993453_38993471delinsGAGCAGGGGCAGGGGCAGC , CM000681.1:g.38993453_38993471delinsGAGCAGGGGCAGGGGCAGC	GRCh37
NC_000019.8:g.43685293_43685311delinsGAGCAGGGGCAGGGGCAGC	NCBI36
NG_008866.1:g.74114_74132delinsGAGCAGGGGCAGGGGCAGC , LRG_766:g.74114_74132delinsGAGCAGGGGCAGGGGCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599547.6:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	ENSP00000471601.2:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
ENST00000359596.8:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC MANE Select	ENSP00000352608.2:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
ENST00000355481.8:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	ENSP00000347667.3:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
ENST00000359596.7:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	ENSP00000352608.2:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
ENST00000360985.7:c.7833-67_7833-49delinsGAGCAGGGGCAGGGGCAGC	ENSP00000354254.4:n.7833-67_7833-49delinsGAGCAGGGGCAGGGGCAGC
ENST00000594335.5:c.1288-67_1288-49delinsGAGCAGGGGCAGGGGCAGC
NM_000540.2:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC , LRG_766t1:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	NP_000531.2:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
NM_001042723.1:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	NP_001036188.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_006723317.1:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_006723380.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_006723319.1:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_006723382.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_011527204.1:c.7833-67_7833-49delinsGAGCAGGGGCAGGGGCAGC	XP_011525506.1:n.7833-67_7833-49delinsGAGCAGGGGCAGGGGCAGC
XM_011527205.1:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_011525507.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_006723317.2:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_006723380.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_006723319.2:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_006723382.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XM_011527205.2:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	XP_011525507.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
XR_001753735.1:n.7919-67_7919-49delinsGAGCAGGGGCAGGGGCAGC
NM_000540.3:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC MANE Select	NP_000531.2:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC
NM_001042723.2:c.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC	NP_001036188.1:n.7836-67_7836-49delinsGAGCAGGGGCAGGGGCAGC