Canonical Allele Identifier: CA1467349385

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741859T= , CM000666.2:g.71741859T=	GRCh38
NC_000004.11:g.72607576T= , CM000666.1:g.72607576T=	GRCh37
NC_000004.10:g.72826440T=	NCBI36
NG_012837.2:g.68662A=
NG_012837.3:g.68662A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*37A= MANE Select	ENSP00000273951.8:n.*37A=
ENST00000273951.12:c.*37A=	ENSP00000273951.8:n.*37A=
ENST00000503364.5:n.135A=
ENST00000503472.5:n.1346A=
ENST00000504199.5:c.*37A=	ENSP00000421725.1:n.*37A=
ENST00000509740.5:c.*285A=	ENSP00000422664.1:n.*285A=
ENST00000513476.5:c.1407A=	ENSP00000426683.1:p.Gly469=
NM_000583.3:c.*37A=	NP_000574.2:n.*37A=
NM_001204306.1:c.*37A=	NP_001191235.1:n.*37A=
NM_001204307.1:c.*37A=	NP_001191236.1:n.*37A=
XM_006714177.2:c.*51A=	XP_006714240.1:n.*51A=
XM_006714177.3:c.*51A=	XP_006714240.1:n.*51A=
NM_000583.4:c.*37A= MANE Select	NP_000574.2:n.*37A=