Canonical Allele Identifier: CA1387393561

Gene: CPOX

Linked Data

• dbSNP Id: rs1707344216

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585496del , CM000665.2:g.98585496del	GRCh38
NC_000003.11:g.98304340del , CM000665.1:g.98304340del	GRCh37
NC_000003.10:g.99787030del	NCBI36
NG_015994.1:g.13116del
NG_015994.2:g.13116del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.3del
ENST00000647941.2:c.1117del MANE Select	ENSP00000497326.1:p.Cys373ValfsTer21
ENST00000264193.2:c.1117del	ENSP00000264193.2:p.Cys373ValfsTer21
ENST00000510489.1:n.367del
ENST00000512905.5:c.3del
NM_000097.5:c.1117del	NP_000088.3:p.Cys373ValfsTer21
XM_005247125.3:c.1117del	XP_005247182.1:p.Cys373ValfsTer22
NM_000097.7:c.1117del MANE Select	NP_000088.3:p.Cys373ValfsTer21
XM_005247125.4:c.1117del	XP_005247182.1:p.Cys373ValfsTer22
XR_001740025.2:n.1288del
XR_001740026.1:n.1852del
XR_001740027.1:n.1392del
XR_001740028.1:n.1358del