Canonical Allele Identifier: CA2545790386

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745626_71745627insTAA , CM000666.2:g.71745626_71745627insTAA	GRCh38
NC_000004.11:g.72611343_72611344insTAA , CM000666.1:g.72611343_72611344insTAA	GRCh37
NC_000004.10:g.72830207_72830208insTAA	NCBI36
NG_012837.2:g.64895_64896insTAT
NG_012837.3:g.64895_64896insTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+525_*25+526insTAT MANE Select	ENSP00000273951.8:n.*25+525_*25+526insTAT
ENST00000273951.12:c.*25+525_*25+526insTAT	ENSP00000273951.8:n.*25+525_*25+526insTAT
ENST00000503364.5:n.123+525_123+526insTAT
ENST00000503472.5:n.1334+525_1334+526insTAT
ENST00000504199.5:c.*25+525_*25+526insTAT	ENSP00000421725.1:n.*25+525_*25+526insTAT
ENST00000509740.5:c.*273+525_*273+526insTAT	ENSP00000422664.1:n.*273+525_*273+526insTAT
ENST00000513476.5:c.1396-3756_1396-3755insTAT	ENSP00000426683.1:n.1396-3756_1396-3755insTAT
NM_000583.3:c.*25+525_*25+526insTAT	NP_000574.2:n.*25+525_*25+526insTAT
NM_001204306.1:c.*25+525_*25+526insTAT	NP_001191235.1:n.*25+525_*25+526insTAT
NM_001204307.1:c.*25+525_*25+526insTAT	NP_001191236.1:n.*25+525_*25+526insTAT
XM_006714177.2:c.*39+525_*39+526insTAT	XP_006714240.1:n.*39+525_*39+526insTAT
XM_006714177.3:c.*39+525_*39+526insTAT	XP_006714240.1:n.*39+525_*39+526insTAT
NM_000583.4:c.*25+525_*25+526insTAT MANE Select	NP_000574.2:n.*25+525_*25+526insTAT