Canonical Allele Identifier: CA1467373288

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756943T= , CM000666.2:g.71756943T=	GRCh38
NC_000004.11:g.72622660T= , CM000666.1:g.72622660T=	GRCh37
NC_000004.10:g.72841524T=	NCBI36
NG_012837.2:g.53578A=
NG_012837.3:g.53578A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.832-29A= MANE Select	ENSP00000273951.8:n.832-29A=
ENST00000273951.12:c.832-29A=	ENSP00000273951.8:n.832-29A=
ENST00000503472.5:n.716-29A=
ENST00000504199.5:c.889-29A=	ENSP00000421725.1:n.889-29A=
ENST00000509740.5:c.832-29A=	ENSP00000422664.1:n.832-29A=
ENST00000513476.5:c.832-29A=	ENSP00000426683.1:n.832-29A=
NM_000583.3:c.832-29A=	NP_000574.2:n.832-29A=
NM_001204306.1:c.832-29A=	NP_001191235.1:n.832-29A=
NM_001204307.1:c.889-29A=	NP_001191236.1:n.889-29A=
XM_006714177.2:c.832-29A=	XP_006714240.1:n.832-29A=
XM_006714177.3:c.832-29A=	XP_006714240.1:n.832-29A=
NM_000583.4:c.832-29A= MANE Select	NP_000574.2:n.832-29A=