Canonical Allele Identifier: CA798103556

Gene: GC

Linked Data

• dbSNP Id: rs1162788359
• MyVariant Identifiers: chr4:g.72611535_72611536del (hg19) ; chr4:g.71745818_71745819del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745819_71745820del , CM000666.2:g.71745819_71745820del	GRCh38
NC_000004.11:g.72611536_72611537del , CM000666.1:g.72611536_72611537del	GRCh37
NC_000004.10:g.72830400_72830401del	NCBI36
NG_012837.2:g.64702_64703del
NG_012837.3:g.64702_64703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+332_*25+333del MANE Select	ENSP00000273951.8:n.*25+332_*25+333del
ENST00000273951.12:c.*25+332_*25+333del	ENSP00000273951.8:n.*25+332_*25+333del
ENST00000503364.5:n.123+332_123+333del
ENST00000503472.5:n.1334+332_1334+333del
ENST00000504199.5:c.*25+332_*25+333del	ENSP00000421725.1:n.*25+332_*25+333del
ENST00000509740.5:c.*273+332_*273+333del	ENSP00000422664.1:n.*273+332_*273+333del
ENST00000513476.5:c.1396-3949_1396-3948del	ENSP00000426683.1:n.1396-3949_1396-3948del
NM_000583.3:c.*25+332_*25+333del	NP_000574.2:n.*25+332_*25+333del
NM_001204306.1:c.*25+332_*25+333del	NP_001191235.1:n.*25+332_*25+333del
NM_001204307.1:c.*25+332_*25+333del	NP_001191236.1:n.*25+332_*25+333del
XM_006714177.2:c.*39+332_*39+333del	XP_006714240.1:n.*39+332_*39+333del
XM_006714177.3:c.*39+332_*39+333del	XP_006714240.1:n.*39+332_*39+333del
NM_000583.4:c.*25+332_*25+333del MANE Select	NP_000574.2:n.*25+332_*25+333del