Canonical Allele Identifier: CA1467349383

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741855T= , CM000666.2:g.71741855T=	GRCh38
NC_000004.11:g.72607572T= , CM000666.1:g.72607572T=	GRCh37
NC_000004.10:g.72826436T=	NCBI36
NG_012837.2:g.68666A=
NG_012837.3:g.68666A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*41A= MANE Select	ENSP00000273951.8:n.*41A=
ENST00000273951.12:c.*41A=	ENSP00000273951.8:n.*41A=
ENST00000503364.5:n.139A=
ENST00000503472.5:n.1350A=
ENST00000504199.5:c.*41A=	ENSP00000421725.1:n.*41A=
ENST00000509740.5:c.*289A=	ENSP00000422664.1:n.*289A=
ENST00000513476.5:c.1411A=	ENSP00000426683.1:p.Thr471=
NM_000583.3:c.*41A=	NP_000574.2:n.*41A=
NM_001204306.1:c.*41A=	NP_001191235.1:n.*41A=
NM_001204307.1:c.*41A=	NP_001191236.1:n.*41A=
XM_006714177.2:c.*55A=	XP_006714240.1:n.*55A=
XM_006714177.3:c.*55A=	XP_006714240.1:n.*55A=
NM_000583.4:c.*41A= MANE Select	NP_000574.2:n.*41A=