Canonical Allele Identifier: CA2740539714
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71756957_71756958insGTAG , CM000666.2:g.71756957_71756958insGTAG GRCh38
NC_000004.11:g.72622674_72622675insGTAG , CM000666.1:g.72622674_72622675insGTAG GRCh37
NC_000004.10:g.72841538_72841539insGTAG NCBI36
NG_012837.2:g.53563_53564insCTAC
NG_012837.3:g.53563_53564insCTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.832-44_832-43insCTAC MANE Select ENSP00000273951.8:n.832-44_832-43insCTAC
ENST00000273951.12:c.832-44_832-43insCTAC ENSP00000273951.8:n.832-44_832-43insCTAC
ENST00000503472.5:n.716-44_716-43insCTAC
ENST00000504199.5:c.889-44_889-43insCTAC ENSP00000421725.1:n.889-44_889-43insCTAC
ENST00000509740.5:c.832-44_832-43insCTAC ENSP00000422664.1:n.832-44_832-43insCTAC
ENST00000513476.5:c.832-44_832-43insCTAC ENSP00000426683.1:n.832-44_832-43insCTAC
NM_000583.3:c.832-44_832-43insCTAC NP_000574.2:n.832-44_832-43insCTAC
NM_001204306.1:c.832-44_832-43insCTAC NP_001191235.1:n.832-44_832-43insCTAC
NM_001204307.1:c.889-44_889-43insCTAC NP_001191236.1:n.889-44_889-43insCTAC
XM_006714177.2:c.832-44_832-43insCTAC XP_006714240.1:n.832-44_832-43insCTAC
XM_006714177.3:c.832-44_832-43insCTAC XP_006714240.1:n.832-44_832-43insCTAC
NM_000583.4:c.832-44_832-43insCTAC MANE Select NP_000574.2:n.832-44_832-43insCTAC