Canonical Allele Identifier: CA2529346174

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745622_71745623del , CM000666.2:g.71745622_71745623del	GRCh38
NC_000004.11:g.72611339_72611340del , CM000666.1:g.72611339_72611340del	GRCh37
NC_000004.10:g.72830203_72830204del	NCBI36
NG_012837.2:g.64898_64899del
NG_012837.3:g.64898_64899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+528_*25+529del MANE Select	ENSP00000273951.8:n.*25+528_*25+529del
ENST00000273951.12:c.*25+528_*25+529del	ENSP00000273951.8:n.*25+528_*25+529del
ENST00000503364.5:n.123+528_123+529del
ENST00000503472.5:n.1334+528_1334+529del
ENST00000504199.5:c.*25+528_*25+529del	ENSP00000421725.1:n.*25+528_*25+529del
ENST00000509740.5:c.*273+528_*273+529del	ENSP00000422664.1:n.*273+528_*273+529del
ENST00000513476.5:c.1396-3753_1396-3752del	ENSP00000426683.1:n.1396-3753_1396-3752del
NM_000583.3:c.*25+528_*25+529del	NP_000574.2:n.*25+528_*25+529del
NM_001204306.1:c.*25+528_*25+529del	NP_001191235.1:n.*25+528_*25+529del
NM_001204307.1:c.*25+528_*25+529del	NP_001191236.1:n.*25+528_*25+529del
XM_006714177.2:c.*39+528_*39+529del	XP_006714240.1:n.*39+528_*39+529del
XM_006714177.3:c.*39+528_*39+529del	XP_006714240.1:n.*39+528_*39+529del
NM_000583.4:c.*25+528_*25+529del MANE Select	NP_000574.2:n.*25+528_*25+529del