Canonical Allele Identifier: CA1467353709

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71751393A= , CM000666.2:g.71751393A=	GRCh38
NC_000004.11:g.72617110A= , CM000666.1:g.72617110A=	GRCh37
NC_000004.10:g.72835974A=	NCBI36
NG_012837.2:g.59128T=
NG_012837.3:g.59128T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1395+1125T= MANE Select	ENSP00000273951.8:n.1395+1125T=
ENST00000273951.12:c.1395+1125T=	ENSP00000273951.8:n.1395+1125T=
ENST00000503364.5:n.68+3018T=
ENST00000503472.5:n.1279+1125T=
ENST00000504199.5:c.1452+1125T=	ENSP00000421725.1:n.1452+1125T=
ENST00000509740.5:c.*218+1125T=	ENSP00000422664.1:n.*218+1125T=
ENST00000513476.5:c.1395+1125T=	ENSP00000426683.1:n.1395+1125T=
NM_000583.3:c.1395+1125T=	NP_000574.2:n.1395+1125T=
NM_001204306.1:c.1395+1125T=	NP_001191235.1:n.1395+1125T=
NM_001204307.1:c.1452+1125T=	NP_001191236.1:n.1452+1125T=
XM_006714177.2:c.1262+3018T=	XP_006714240.1:n.1262+3018T=
XM_006714177.3:c.1262+3018T=	XP_006714240.1:n.1262+3018T=
NM_000583.4:c.1395+1125T= MANE Select	NP_000574.2:n.1395+1125T=