Canonical Allele Identifier: CA1387393622

Gene: CPOX

Linked Data

• dbSNP Id: rs1707345531

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585549_98585568del , CM000665.2:g.98585549_98585568del	GRCh38
NC_000003.11:g.98304393_98304412del , CM000665.1:g.98304393_98304412del	GRCh37
NC_000003.10:g.99787083_99787102del	NCBI36
NG_015994.1:g.13047_13066del
NG_015994.2:g.13047_13066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1048_1067del MANE Select	ENSP00000497326.1:p.Val350LeufsTer18
ENST00000264193.2:c.1048_1067del	ENSP00000264193.2:p.Val350LeufsTer18
ENST00000510489.1:n.298_317del
NM_000097.5:c.1048_1067del	NP_000088.3:p.Val350LeufsTer18
XM_005247125.3:c.1048_1067del	XP_005247182.1:p.Val350LeufsTer18
NM_000097.7:c.1048_1067del MANE Select	NP_000088.3:p.Val350LeufsTer18
XM_005247125.4:c.1048_1067del	XP_005247182.1:p.Val350LeufsTer18
XR_001740025.2:n.1219_1238del
XR_001740026.1:n.1783_1802del
XR_001740027.1:n.1323_1342del
XR_001740028.1:n.1289_1308del