Canonical Allele Identifier: CA1467385934
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71784755_71784759delinsAAGTT , CM000666.2:g.71784755_71784759delinsAAGTT GRCh38
NC_000004.11:g.72650472_72650476delinsAAGTT , CM000666.1:g.72650472_72650476delinsAAGTT GRCh37
NC_000004.10:g.72869336_72869340delinsAAGTT NCBI36
NG_012837.2:g.25762_25766delinsAACTT
NG_012837.3:g.25762_25766delinsAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000504199.5:c.22-705_22-701delinsAACTT ENSP00000421725.1:n.22-705_22-701delinsAACTT
ENST00000506245.1:c.-36-705_-36-701delinsAACTT ENSP00000426718.1:n.-36-705_-36-701delinsAACTT
NM_001204306.1:c.-36-705_-36-701delinsAACTT NP_001191235.1:n.-36-705_-36-701delinsAACTT
NM_001204307.1:c.22-705_22-701delinsAACTT NP_001191236.1:n.22-705_22-701delinsAACTT