Canonical Allele Identifier: CA1467385632

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784057G= , CM000666.2:g.71784057G=	GRCh38
NC_000004.11:g.72649774G= , CM000666.1:g.72649774G=	GRCh37
NC_000004.10:g.72868638G=	NCBI36
NG_012837.2:g.26464C=
NG_012837.3:g.26464C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.-39C= MANE Select	ENSP00000273951.8:n.-39C=
ENST00000273951.12:c.-39C=	ENSP00000273951.8:n.-39C=
ENST00000504199.5:c.22-3C=	ENSP00000421725.1:n.22-3C=
ENST00000506245.1:c.-36-3C=	ENSP00000426718.1:n.-36-3C=
ENST00000509740.5:c.-39C=	ENSP00000422664.1:n.-39C=
NM_000583.3:c.-39C=	NP_000574.2:n.-39C=
NM_001204306.1:c.-36-3C=	NP_001191235.1:n.-36-3C=
NM_001204307.1:c.22-3C=	NP_001191236.1:n.22-3C=
XM_006714177.2:c.-39C=	XP_006714240.1:n.-39C=
XM_006714177.3:c.-39C=	XP_006714240.1:n.-39C=
NM_000583.4:c.-39C= MANE Select	NP_000574.2:n.-39C=