Canonical Allele Identifier: CA1467351247

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745807_71745810delinsTTGA , CM000666.2:g.71745807_71745810delinsTTGA	GRCh38
NC_000004.11:g.72611524_72611527delinsTTGA , CM000666.1:g.72611524_72611527delinsTTGA	GRCh37
NC_000004.10:g.72830388_72830391delinsTTGA	NCBI36
NG_012837.2:g.64711_64714delinsTCAA
NG_012837.3:g.64711_64714delinsTCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+341_*25+344delinsTCAA MANE Select	ENSP00000273951.8:n.*25+341_*25+344delinsTCAA
ENST00000273951.12:c.*25+341_*25+344delinsTCAA	ENSP00000273951.8:n.*25+341_*25+344delinsTCAA
ENST00000503364.5:n.123+341_123+344delinsTCAA
ENST00000503472.5:n.1334+341_1334+344delinsTCAA
ENST00000504199.5:c.*25+341_*25+344delinsTCAA	ENSP00000421725.1:n.*25+341_*25+344delinsTCAA
ENST00000509740.5:c.*273+341_*273+344delinsTCAA	ENSP00000422664.1:n.*273+341_*273+344delinsTCAA
ENST00000513476.5:c.1396-3940_1396-3937delinsTCAA	ENSP00000426683.1:n.1396-3940_1396-3937delinsTCAA
NM_000583.3:c.*25+341_*25+344delinsTCAA	NP_000574.2:n.*25+341_*25+344delinsTCAA
NM_001204306.1:c.*25+341_*25+344delinsTCAA	NP_001191235.1:n.*25+341_*25+344delinsTCAA
NM_001204307.1:c.*25+341_*25+344delinsTCAA	NP_001191236.1:n.*25+341_*25+344delinsTCAA
XM_006714177.2:c.*39+341_*39+344delinsTCAA	XP_006714240.1:n.*39+341_*39+344delinsTCAA
XM_006714177.3:c.*39+341_*39+344delinsTCAA	XP_006714240.1:n.*39+341_*39+344delinsTCAA
NM_000583.4:c.*25+341_*25+344delinsTCAA MANE Select	NP_000574.2:n.*25+341_*25+344delinsTCAA