Canonical Allele Identifier: CA1467351221

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745745_71745746delinsGT , CM000666.2:g.71745745_71745746delinsGT	GRCh38
NC_000004.11:g.72611462_72611463delinsGT , CM000666.1:g.72611462_72611463delinsGT	GRCh37
NC_000004.10:g.72830326_72830327delinsGT	NCBI36
NG_012837.2:g.64775_64776delinsAC
NG_012837.3:g.64775_64776delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+405_*25+406delinsAC MANE Select	ENSP00000273951.8:n.*25+405_*25+406delinsAC
ENST00000273951.12:c.*25+405_*25+406delinsAC	ENSP00000273951.8:n.*25+405_*25+406delinsAC
ENST00000503364.5:n.123+405_123+406delinsAC
ENST00000503472.5:n.1334+405_1334+406delinsAC
ENST00000504199.5:c.*25+405_*25+406delinsAC	ENSP00000421725.1:n.*25+405_*25+406delinsAC
ENST00000509740.5:c.*273+405_*273+406delinsAC	ENSP00000422664.1:n.*273+405_*273+406delinsAC
ENST00000513476.5:c.1396-3876_1396-3875delinsAC	ENSP00000426683.1:n.1396-3876_1396-3875delinsAC
NM_000583.3:c.*25+405_*25+406delinsAC	NP_000574.2:n.*25+405_*25+406delinsAC
NM_001204306.1:c.*25+405_*25+406delinsAC	NP_001191235.1:n.*25+405_*25+406delinsAC
NM_001204307.1:c.*25+405_*25+406delinsAC	NP_001191236.1:n.*25+405_*25+406delinsAC
XM_006714177.2:c.*39+405_*39+406delinsAC	XP_006714240.1:n.*39+405_*39+406delinsAC
XM_006714177.3:c.*39+405_*39+406delinsAC	XP_006714240.1:n.*39+405_*39+406delinsAC
NM_000583.4:c.*25+405_*25+406delinsAC MANE Select	NP_000574.2:n.*25+405_*25+406delinsAC