Canonical Allele Identifier: CA1467351286
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71745901G= , CM000666.2:g.71745901G= GRCh38
NC_000004.11:g.72611618G= , CM000666.1:g.72611618G= GRCh37
NC_000004.10:g.72830482G= NCBI36
NG_012837.2:g.64620C=
NG_012837.3:g.64620C=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*25+250C= MANE Select ENSP00000273951.8:n.*25+250C=
ENST00000273951.12:c.*25+250C= ENSP00000273951.8:n.*25+250C=
ENST00000503364.5:n.123+250C=
ENST00000503472.5:n.1334+250C=
ENST00000504199.5:c.*25+250C= ENSP00000421725.1:n.*25+250C=
ENST00000509740.5:c.*273+250C= ENSP00000422664.1:n.*273+250C=
ENST00000513476.5:c.1396-4031C= ENSP00000426683.1:n.1396-4031C=
NM_000583.3:c.*25+250C= NP_000574.2:n.*25+250C=
NM_001204306.1:c.*25+250C= NP_001191235.1:n.*25+250C=
NM_001204307.1:c.*25+250C= NP_001191236.1:n.*25+250C=
XM_006714177.2:c.*39+250C= XP_006714240.1:n.*39+250C=
XM_006714177.3:c.*39+250C= XP_006714240.1:n.*39+250C=
NM_000583.4:c.*25+250C= MANE Select NP_000574.2:n.*25+250C=