Canonical Allele Identifier: CA1467351330
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71746009_71746011delinsTCG , CM000666.2:g.71746009_71746011delinsTCG GRCh38
NC_000004.11:g.72611726_72611728delinsTCG , CM000666.1:g.72611726_72611728delinsTCG GRCh37
NC_000004.10:g.72830590_72830592delinsTCG NCBI36
NG_012837.2:g.64510_64512delinsCGA
NG_012837.3:g.64510_64512delinsCGA

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*25+140_*25+142delinsCGA MANE Select ENSP00000273951.8:n.*25+140_*25+142delins...
ENST00000273951.12:c.*25+140_*25+142delinsCGA ENSP00000273951.8:n.*25+140_*25+142delins...
ENST00000503364.5:n.123+140_123+142delinsCGA
ENST00000503472.5:n.1334+140_1334+142delinsCGA
ENST00000504199.5:c.*25+140_*25+142delinsCGA ENSP00000421725.1:n.*25+140_*25+142delins...
ENST00000509740.5:c.*273+140_*273+142delinsCGA ENSP00000422664.1:n.*273+140_*273+142deli...
ENST00000513476.5:c.1396-4141_1396-4139delinsCGA ENSP00000426683.1:n.1396-4141_1396-4139de...
NM_000583.3:c.*25+140_*25+142delinsCGA NP_000574.2:n.*25+140_*25+142delinsCGA
NM_001204306.1:c.*25+140_*25+142delinsCGA NP_001191235.1:n.*25+140_*25+142delinsCGA...
NM_001204307.1:c.*25+140_*25+142delinsCGA NP_001191236.1:n.*25+140_*25+142delinsCGA...
XM_006714177.2:c.*39+140_*39+142delinsCGA XP_006714240.1:n.*39+140_*39+142delinsCGA...
XM_006714177.3:c.*39+140_*39+142delinsCGA XP_006714240.1:n.*39+140_*39+142delinsCGA...
NM_000583.4:c.*25+140_*25+142delinsCGA MANE Select NP_000574.2:n.*25+140_*25+142delinsCGA