Canonical Allele Identifier: CA1467373221

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756826T= , CM000666.2:g.71756826T=	GRCh38
NC_000004.11:g.72622543T= , CM000666.1:g.72622543T=	GRCh37
NC_000004.10:g.72841407T=	NCBI36
NG_012837.2:g.53695A=
NG_012837.3:g.53695A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.920A= MANE Select	ENSP00000273951.8:p.Asp307=
ENST00000273951.12:c.920A=	ENSP00000273951.8:p.Asp307=
ENST00000503472.5:n.804A=
ENST00000504199.5:c.977A=	ENSP00000421725.1:p.Asp326=
ENST00000509740.5:c.920A=	ENSP00000422664.1:p.Asp307=
ENST00000513476.5:c.920A=	ENSP00000426683.1:p.Asp307=
NM_000583.3:c.920A=	NP_000574.2:p.Asp307=
NM_001204306.1:c.920A=	NP_001191235.1:p.Asp307=
NM_001204307.1:c.977A=	NP_001191236.1:p.Asp326=
XM_006714177.2:c.920A=	XP_006714240.1:p.Asp307=
XM_006714177.3:c.920A=	XP_006714240.1:p.Asp307=
NM_000583.4:c.920A= MANE Select	NP_000574.2:p.Asp307=