Canonical Allele Identifier: CA1467385258

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71783207C= , CM000666.2:g.71783207C=	GRCh38
NC_000004.11:g.72648924C= , CM000666.1:g.72648924C=	GRCh37
NC_000004.10:g.72867788C=	NCBI36
NG_012837.2:g.27314G=
NG_012837.3:g.27314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.58+754G= MANE Select	ENSP00000273951.8:n.58+754G=
ENST00000273951.12:c.58+754G=	ENSP00000273951.8:n.58+754G=
ENST00000504199.5:c.115+754G=	ENSP00000421725.1:n.115+754G=
ENST00000506245.1:c.58+754G=	ENSP00000426718.1:n.58+754G=
ENST00000509740.5:c.58+754G=	ENSP00000422664.1:n.58+754G=
ENST00000513476.5:c.58+754G=	ENSP00000426683.1:n.58+754G=
NM_000583.3:c.58+754G=	NP_000574.2:n.58+754G=
NM_001204306.1:c.58+754G=	NP_001191235.1:n.58+754G=
NM_001204307.1:c.115+754G=	NP_001191236.1:n.115+754G=
XM_006714177.2:c.58+754G=	XP_006714240.1:n.58+754G=
XM_006714177.3:c.58+754G=	XP_006714240.1:n.58+754G=
NM_000583.4:c.58+754G= MANE Select	NP_000574.2:n.58+754G=