Canonical Allele Identifier: CA798103611

Gene: GC

Linked Data

• dbSNP Id: rs1296500292
• MyVariant Identifiers: chr4:g.72611632del (hg19) ; chr4:g.71745915del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745916del , CM000666.2:g.71745916del	GRCh38
NC_000004.11:g.72611633del , CM000666.1:g.72611633del	GRCh37
NC_000004.10:g.72830497del	NCBI36
NG_012837.2:g.64606del
NG_012837.3:g.64606del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*25+236del MANE Select	ENSP00000273951.8:n.*25+236del
ENST00000273951.12:c.*25+236del	ENSP00000273951.8:n.*25+236del
ENST00000503364.5:n.123+236del
ENST00000503472.5:n.1334+236del
ENST00000504199.5:c.*25+236del	ENSP00000421725.1:n.*25+236del
ENST00000509740.5:c.*273+236del	ENSP00000422664.1:n.*273+236del
ENST00000513476.5:c.1396-4045del	ENSP00000426683.1:n.1396-4045del
NM_000583.3:c.*25+236del	NP_000574.2:n.*25+236del
NM_001204306.1:c.*25+236del	NP_001191235.1:n.*25+236del
NM_001204307.1:c.*25+236del	NP_001191236.1:n.*25+236del
XM_006714177.2:c.*39+236del	XP_006714240.1:n.*39+236del
XM_006714177.3:c.*39+236del	XP_006714240.1:n.*39+236del
NM_000583.4:c.*25+236del MANE Select	NP_000574.2:n.*25+236del