Canonical Allele Identifier: CA552290270

Gene: GC

Linked Data

• dbSNP Id: rs1438467226
• gnomAD v2: 4-72621657-CTATT-C
• gnomAD v3: 4-71755940-CTATT-C
• gnomAD v4: 4-71755940-CTATT-C
• MyVariant Identifiers: chr4:g.72621658_72621661del (hg19) ; chr4:g.71755941_71755944del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755942_71755945del , CM000666.2:g.71755942_71755945del	GRCh38
NC_000004.11:g.72621659_72621662del , CM000666.1:g.72621659_72621662del	GRCh37
NC_000004.10:g.72840523_72840526del	NCBI36
NG_012837.2:g.54577_54580del
NG_012837.3:g.54577_54580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1034+768_1034+771del MANE Select	ENSP00000273951.8:n.1034+768_1034+771del
ENST00000273951.12:c.1034+768_1034+771del	ENSP00000273951.8:n.1034+768_1034+771del
ENST00000503472.5:n.918+768_918+771del
ENST00000504199.5:c.1091+768_1091+771del	ENSP00000421725.1:n.1091+768_1091+771del
ENST00000509740.5:c.1034+768_1034+771del	ENSP00000422664.1:n.1034+768_1034+771del
ENST00000513476.5:c.1034+768_1034+771del	ENSP00000426683.1:n.1034+768_1034+771del
NM_000583.3:c.1034+768_1034+771del	NP_000574.2:n.1034+768_1034+771del
NM_001204306.1:c.1034+768_1034+771del	NP_001191235.1:n.1034+768_1034+771del
NM_001204307.1:c.1091+768_1091+771del	NP_001191236.1:n.1091+768_1091+771del
XM_006714177.2:c.1034+768_1034+771del	XP_006714240.1:n.1034+768_1034+771del
XM_006714177.3:c.1034+768_1034+771del	XP_006714240.1:n.1034+768_1034+771del
NM_000583.4:c.1034+768_1034+771del MANE Select	NP_000574.2:n.1034+768_1034+771del