Canonical Allele Identifier: CA1467351142

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745580_71745583delinsATTG , CM000666.2:g.71745580_71745583delinsATTG	GRCh38
NC_000004.11:g.72611297_72611300delinsATTG , CM000666.1:g.72611297_72611300delinsATTG	GRCh37
NC_000004.10:g.72830161_72830164delinsATTG	NCBI36
NG_012837.2:g.64938_64941delinsCAAT
NG_012837.3:g.64938_64941delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+568_*25+571delinsCAAT MANE Select	ENSP00000273951.8:n.*25+568_*25+571delinsCAAT
ENST00000273951.12:c.*25+568_*25+571delinsCAAT	ENSP00000273951.8:n.*25+568_*25+571delinsCAAT
ENST00000503364.5:n.123+568_123+571delinsCAAT
ENST00000503472.5:n.1334+568_1334+571delinsCAAT
ENST00000504199.5:c.*25+568_*25+571delinsCAAT	ENSP00000421725.1:n.*25+568_*25+571delinsCAAT
ENST00000509740.5:c.*273+568_*273+571delinsCAAT	ENSP00000422664.1:n.*273+568_*273+571delinsCAAT
ENST00000513476.5:c.1396-3713_1396-3710delinsCAAT	ENSP00000426683.1:n.1396-3713_1396-3710delinsCAAT
NM_000583.3:c.*25+568_*25+571delinsCAAT	NP_000574.2:n.*25+568_*25+571delinsCAAT
NM_001204306.1:c.*25+568_*25+571delinsCAAT	NP_001191235.1:n.*25+568_*25+571delinsCAAT
NM_001204307.1:c.*25+568_*25+571delinsCAAT	NP_001191236.1:n.*25+568_*25+571delinsCAAT
XM_006714177.2:c.*39+568_*39+571delinsCAAT	XP_006714240.1:n.*39+568_*39+571delinsCAAT
XM_006714177.3:c.*39+568_*39+571delinsCAAT	XP_006714240.1:n.*39+568_*39+571delinsCAAT
NM_000583.4:c.*25+568_*25+571delinsCAAT MANE Select	NP_000574.2:n.*25+568_*25+571delinsCAAT