Canonical Allele Identifier: CA1467386091
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71785136_71785139delinsTGTG , CM000666.2:g.71785136_71785139delinsTGTG GRCh38
NC_000004.11:g.72650853_72650856delinsTGTG , CM000666.1:g.72650853_72650856delinsTGTG GRCh37
NC_000004.10:g.72869717_72869720delinsTGTG NCBI36
NG_012837.2:g.25382_25385delinsCACA
NG_012837.3:g.25382_25385delinsCACA

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-1085_22-1082delinsCACA ENSP00000421725.1:n.22-1085_22-1082delinsCACA
ENST00000506245.1:c.-37+781_-37+784delinsCACA ENSP00000426718.1:n.-37+781_-37+784delinsCACA
NM_001204306.1:c.-36-1085_-36-1082delinsCACA NP_001191235.1:n.-36-1085_-36-1082delinsCACA
NM_001204307.1:c.22-1085_22-1082delinsCACA NP_001191236.1:n.22-1085_22-1082delinsCACA