Canonical Allele Identifier: CA1467385947
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784781_71784782delinsTA , CM000666.2:g.71784781_71784782delinsTA GRCh38
NC_000004.11:g.72650498_72650499delinsTA , CM000666.1:g.72650498_72650499delinsTA GRCh37
NC_000004.10:g.72869362_72869363delinsTA NCBI36
NG_012837.2:g.25739_25740delinsTA
NG_012837.3:g.25739_25740delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-728_22-727delinsTA ENSP00000421725.1:n.22-728_22-727delinsTA
ENST00000506245.1:c.-36-728_-36-727delinsTA ENSP00000426718.1:n.-36-728_-36-727delinsTA
NM_001204306.1:c.-36-728_-36-727delinsTA NP_001191235.1:n.-36-728_-36-727delinsTA
NM_001204307.1:c.22-728_22-727delinsTA NP_001191236.1:n.22-728_22-727delinsTA