Canonical Allele Identifier: CA1467349632

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742439A= , CM000666.2:g.71742439A=	GRCh38
NC_000004.11:g.72608156A= , CM000666.1:g.72608156A=	GRCh37
NC_000004.10:g.72827020A=	NCBI36
NG_012837.2:g.68082T=
NG_012837.3:g.68082T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-569T= MANE Select	ENSP00000273951.8:n.*26-569T=
ENST00000273951.12:c.*26-569T=	ENSP00000273951.8:n.*26-569T=
ENST00000503364.5:n.124-569T=
ENST00000503472.5:n.1335-569T=
ENST00000504199.5:c.*26-569T=	ENSP00000421725.1:n.*26-569T=
ENST00000509740.5:c.*274-569T=	ENSP00000422664.1:n.*274-569T=
ENST00000513476.5:c.1396-569T=	ENSP00000426683.1:n.1396-569T=
NM_000583.3:c.*26-569T=	NP_000574.2:n.*26-569T=
NM_001204306.1:c.*26-569T=	NP_001191235.1:n.*26-569T=
NM_001204307.1:c.*26-569T=	NP_001191236.1:n.*26-569T=
XM_006714177.2:c.*40-569T=	XP_006714240.1:n.*40-569T=
XM_006714177.3:c.*40-569T=	XP_006714240.1:n.*40-569T=
NM_000583.4:c.*26-569T= MANE Select	NP_000574.2:n.*26-569T=