Canonical Allele Identifier: CA1467351295
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71745914_71745915delinsGA , CM000666.2:g.71745914_71745915delinsGA GRCh38
NC_000004.11:g.72611631_72611632delinsGA , CM000666.1:g.72611631_72611632delinsGA GRCh37
NC_000004.10:g.72830495_72830496delinsGA NCBI36
NG_012837.2:g.64606_64607delinsTC
NG_012837.3:g.64606_64607delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*25+236_*25+237delinsTC MANE Select ENSP00000273951.8:n.*25+236_*25+237delins...
ENST00000273951.12:c.*25+236_*25+237delinsTC ENSP00000273951.8:n.*25+236_*25+237delins...
ENST00000503364.5:n.123+236_123+237delinsTC
ENST00000503472.5:n.1334+236_1334+237delinsTC
ENST00000504199.5:c.*25+236_*25+237delinsTC ENSP00000421725.1:n.*25+236_*25+237delins...
ENST00000509740.5:c.*273+236_*273+237delinsTC ENSP00000422664.1:n.*273+236_*273+237deli...
ENST00000513476.5:c.1396-4045_1396-4044delinsTC ENSP00000426683.1:n.1396-4045_1396-4044de...
NM_000583.3:c.*25+236_*25+237delinsTC NP_000574.2:n.*25+236_*25+237delinsTC
NM_001204306.1:c.*25+236_*25+237delinsTC NP_001191235.1:n.*25+236_*25+237delinsTC
NM_001204307.1:c.*25+236_*25+237delinsTC NP_001191236.1:n.*25+236_*25+237delinsTC
XM_006714177.2:c.*39+236_*39+237delinsTC XP_006714240.1:n.*39+236_*39+237delinsTC
XM_006714177.3:c.*39+236_*39+237delinsTC XP_006714240.1:n.*39+236_*39+237delinsTC
NM_000583.4:c.*25+236_*25+237delinsTC MANE Select NP_000574.2:n.*25+236_*25+237delinsTC