Canonical Allele Identifier: CA1467372904

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756108_71756110delinsGAA , CM000666.2:g.71756108_71756110delinsGAA	GRCh38
NC_000004.11:g.72621825_72621827delinsGAA , CM000666.1:g.72621825_72621827delinsGAA	GRCh37
NC_000004.10:g.72840689_72840691delinsGAA	NCBI36
NG_012837.2:g.54411_54413delinsTTC
NG_012837.3:g.54411_54413delinsTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1034+602_1034+604delinsTTC MANE Select	ENSP00000273951.8:n.1034+602_1034+604delinsTTC
ENST00000273951.12:c.1034+602_1034+604delinsTTC	ENSP00000273951.8:n.1034+602_1034+604delinsTTC
ENST00000503472.5:n.918+602_918+604delinsTTC
ENST00000504199.5:c.1091+602_1091+604delinsTTC	ENSP00000421725.1:n.1091+602_1091+604delinsTTC
ENST00000509740.5:c.1034+602_1034+604delinsTTC	ENSP00000422664.1:n.1034+602_1034+604delinsTTC
ENST00000513476.5:c.1034+602_1034+604delinsTTC	ENSP00000426683.1:n.1034+602_1034+604delinsTTC
NM_000583.3:c.1034+602_1034+604delinsTTC	NP_000574.2:n.1034+602_1034+604delinsTTC
NM_001204306.1:c.1034+602_1034+604delinsTTC	NP_001191235.1:n.1034+602_1034+604delinsTTC
NM_001204307.1:c.1091+602_1091+604delinsTTC	NP_001191236.1:n.1091+602_1091+604delinsTTC
XM_006714177.2:c.1034+602_1034+604delinsTTC	XP_006714240.1:n.1034+602_1034+604delinsTTC
XM_006714177.3:c.1034+602_1034+604delinsTTC	XP_006714240.1:n.1034+602_1034+604delinsTTC
NM_000583.4:c.1034+602_1034+604delinsTTC MANE Select	NP_000574.2:n.1034+602_1034+604delinsTTC