Canonical Allele Identifier: CA1467353636
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71751228A= , CM000666.2:g.71751228A= GRCh38
NC_000004.11:g.72616945A= , CM000666.1:g.72616945A= GRCh37
NC_000004.10:g.72835809A= NCBI36
NG_012837.2:g.59293T=
NG_012837.3:g.59293T=

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1395+1290T= MANE Select ENSP00000273951.8:p.=
ENST00000273951.12:c.1395+1290T= ENSP00000273951.8:p.=
ENST00000503364.5:n.68+3183T=
ENST00000503472.5:n.1279+1290T=
ENST00000504199.5:c.1452+1290T= ENSP00000421725.1:p.=
ENST00000509740.5:c.*218+1290T= ENSP00000422664.1:p.=
ENST00000513476.5:c.1395+1290T= ENSP00000426683.1:p.=
NM_000583.3:c.1395+1290T= NP_000574.2:p.=
NM_001204306.1:c.1395+1290T= NP_001191235.1:p.=
NM_001204307.1:c.1452+1290T= NP_001191236.1:p.=
XM_006714177.2:c.1262+3183T= XP_006714240.1:p.=
XM_006714177.3:c.1262+3183T= XP_006714240.1:p.=
NM_000583.4:c.1395+1290T= MANE Select NP_000574.2:p.=