Canonical Allele Identifier: CA1467353648
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs1741546409

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71751259dup , CM000666.2:g.71751259dup GRCh38
NC_000004.11:g.72616976dup , CM000666.1:g.72616976dup GRCh37
NC_000004.10:g.72835840dup NCBI36
NG_012837.2:g.59262dup
NG_012837.3:g.59262dup

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1395+1259dup MANE Select ENSP00000273951.8:p.=
ENST00000273951.12:c.1395+1259dup ENSP00000273951.8:p.=
ENST00000503364.5:n.68+3152dup
ENST00000503472.5:n.1279+1259dup
ENST00000504199.5:c.1452+1259dup ENSP00000421725.1:p.=
ENST00000509740.5:c.*218+1259dup ENSP00000422664.1:p.=
ENST00000513476.5:c.1395+1259dup ENSP00000426683.1:p.=
NM_000583.3:c.1395+1259dup NP_000574.2:p.=
NM_001204306.1:c.1395+1259dup NP_001191235.1:p.=
NM_001204307.1:c.1452+1259dup NP_001191236.1:p.=
XM_006714177.2:c.1262+3152dup XP_006714240.1:p.=
XM_006714177.3:c.1262+3152dup XP_006714240.1:p.=
NM_000583.4:c.1395+1259dup MANE Select NP_000574.2:p.=