Canonical Allele Identifier: CA2563831594

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745613_71745614insC , CM000666.2:g.71745613_71745614insC	GRCh38
NC_000004.11:g.72611330_72611331insC , CM000666.1:g.72611330_72611331insC	GRCh37
NC_000004.10:g.72830194_72830195insC	NCBI36
NG_012837.2:g.64907_64908insG
NG_012837.3:g.64907_64908insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+537_*25+538insG MANE Select	ENSP00000273951.8:n.*25+537_*25+538insG
ENST00000273951.12:c.*25+537_*25+538insG	ENSP00000273951.8:n.*25+537_*25+538insG
ENST00000503364.5:n.123+537_123+538insG
ENST00000503472.5:n.1334+537_1334+538insG
ENST00000504199.5:c.*25+537_*25+538insG	ENSP00000421725.1:n.*25+537_*25+538insG
ENST00000509740.5:c.*273+537_*273+538insG	ENSP00000422664.1:n.*273+537_*273+538insG
ENST00000513476.5:c.1396-3744_1396-3743insG	ENSP00000426683.1:n.1396-3744_1396-3743insG
NM_000583.3:c.*25+537_*25+538insG	NP_000574.2:n.*25+537_*25+538insG
NM_001204306.1:c.*25+537_*25+538insG	NP_001191235.1:n.*25+537_*25+538insG
NM_001204307.1:c.*25+537_*25+538insG	NP_001191236.1:n.*25+537_*25+538insG
XM_006714177.2:c.*39+537_*39+538insG	XP_006714240.1:n.*39+537_*39+538insG
XM_006714177.3:c.*39+537_*39+538insG	XP_006714240.1:n.*39+537_*39+538insG
NM_000583.4:c.*25+537_*25+538insG MANE Select	NP_000574.2:n.*25+537_*25+538insG