Canonical Allele Identifier: CA357201274

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71752617A>T , CM000666.2:g.71752617A>T	GRCh38
NC_000004.11:g.72618334A>T , CM000666.1:g.72618334A>T	GRCh37
NC_000004.10:g.72837198A>T	NCBI36
NG_012837.2:g.57904T>A
NG_012837.3:g.57904T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000583.4:c.1296T>A MANE Select	NP_000574.2:p.Asp432Glu
ENST00000273951.13:c.1296T>A MANE Select	ENSP00000273951.8:p.Asp432Glu
NM_000583.3:c.1296T>A	NP_000574.2:p.Asp432Glu
NM_001204306.1:c.1296T>A	NP_001191235.1:p.Asp432Glu
NM_001204307.1:c.1353T>A	NP_001191236.1:p.Asp451Glu
ENST00000273951.12:c.1296T>A	ENSP00000273951.8:p.Asp432Glu
ENST00000503364.5:n.68+1794T>A
ENST00000503472.5:n.1180T>A
ENST00000504199.5:c.1353T>A	ENSP00000421725.1:p.Asp451Glu
ENST00000509740.5:c.*119T>A	ENSP00000422664.1:n.*119T>A
ENST00000513476.5:c.1296T>A	ENSP00000426683.1:p.Asp432Glu
XM_006714177.2:c.1262+1794T>A	XP_006714240.1:n.1262+1794T>A
XM_006714177.3:c.1262+1794T>A	XP_006714240.1:n.1262+1794T>A