Canonical Allele Identifier: CA1467351252

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745817_71745819delinsCTG , CM000666.2:g.71745817_71745819delinsCTG	GRCh38
NC_000004.11:g.72611534_72611536delinsCTG , CM000666.1:g.72611534_72611536delinsCTG	GRCh37
NC_000004.10:g.72830398_72830400delinsCTG	NCBI36
NG_012837.2:g.64702_64704delinsCAG
NG_012837.3:g.64702_64704delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+332_*25+334delinsCAG MANE Select	ENSP00000273951.8:n.*25+332_*25+334delinsCAG
ENST00000273951.12:c.*25+332_*25+334delinsCAG	ENSP00000273951.8:n.*25+332_*25+334delinsCAG
ENST00000503364.5:n.123+332_123+334delinsCAG
ENST00000503472.5:n.1334+332_1334+334delinsCAG
ENST00000504199.5:c.*25+332_*25+334delinsCAG	ENSP00000421725.1:n.*25+332_*25+334delinsCAG
ENST00000509740.5:c.*273+332_*273+334delinsCAG	ENSP00000422664.1:n.*273+332_*273+334delinsCAG
ENST00000513476.5:c.1396-3949_1396-3947delinsCAG	ENSP00000426683.1:n.1396-3949_1396-3947delinsCAG
NM_000583.3:c.*25+332_*25+334delinsCAG	NP_000574.2:n.*25+332_*25+334delinsCAG
NM_001204306.1:c.*25+332_*25+334delinsCAG	NP_001191235.1:n.*25+332_*25+334delinsCAG
NM_001204307.1:c.*25+332_*25+334delinsCAG	NP_001191236.1:n.*25+332_*25+334delinsCAG
XM_006714177.2:c.*39+332_*39+334delinsCAG	XP_006714240.1:n.*39+332_*39+334delinsCAG
XM_006714177.3:c.*39+332_*39+334delinsCAG	XP_006714240.1:n.*39+332_*39+334delinsCAG
NM_000583.4:c.*25+332_*25+334delinsCAG MANE Select	NP_000574.2:n.*25+332_*25+334delinsCAG