Canonical Allele Identifier: CA1467386042
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784987_71784994delinsCTGGTTTT , CM000666.2:g.71784987_71784994delinsCTGGTTTT GRCh38
NC_000004.11:g.72650704_72650711delinsCTGGTTTT , CM000666.1:g.72650704_72650711delinsCTGGTTTT GRCh37
NC_000004.10:g.72869568_72869575delinsCTGGTTTT NCBI36
NG_012837.2:g.25527_25534delinsAAAACCAG
NG_012837.3:g.25527_25534delinsAAAACCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000504199.5:c.22-940_22-933delinsAAAACCAG ENSP00000421725.1:n.22-940_22-933delinsAA...
ENST00000506245.1:c.-37+926_-36-933delinsAAAACCAG ENSP00000426718.1:n.-37+926_-36-933delins...
NM_001204306.1:c.-36-940_-36-933delinsAAAACCAG NP_001191235.1:n.-36-940_-36-933delinsAAA...
NM_001204307.1:c.22-940_22-933delinsAAAACCAG NP_001191236.1:n.22-940_22-933delinsAAAAC...