Canonical Allele Identifier: CA1467373189

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756757G= , CM000666.2:g.71756757G=	GRCh38
NC_000004.11:g.72622474G= , CM000666.1:g.72622474G=	GRCh37
NC_000004.10:g.72841338G=	NCBI36
NG_012837.2:g.53764C=
NG_012837.3:g.53764C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.989C= MANE Select	ENSP00000273951.8:p.Thr330=
ENST00000273951.12:c.989C=	ENSP00000273951.8:p.Thr330=
ENST00000503472.5:n.873C=
ENST00000504199.5:c.1046C=	ENSP00000421725.1:p.Thr349=
ENST00000509740.5:c.989C=	ENSP00000422664.1:p.Thr330=
ENST00000513476.5:c.989C=	ENSP00000426683.1:p.Thr330=
NM_000583.3:c.989C=	NP_000574.2:p.Thr330=
NM_001204306.1:c.989C=	NP_001191235.1:p.Thr330=
NM_001204307.1:c.1046C=	NP_001191236.1:p.Thr349=
XM_006714177.2:c.989C=	XP_006714240.1:p.Thr330=
XM_006714177.3:c.989C=	XP_006714240.1:p.Thr330=
NM_000583.4:c.989C= MANE Select	NP_000574.2:p.Thr330=