Canonical Allele Identifier: CA2586965845
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585514del , CM000665.2:g.98585514del GRCh38
NC_000003.11:g.98304358del , CM000665.1:g.98304358del GRCh37
NC_000003.10:g.99787048del NCBI36
NG_015994.1:g.13101del
NG_015994.2:g.13101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1102del MANE Select ENSP00000497326.1:p.Val369Ter
ENST00000264193.2:c.1102del ENSP00000264193.2:p.Val369Ter
ENST00000510489.1:n.352del
NM_000097.5:c.1102del NP_000088.3:p.Val369Ter
XM_005247125.3:c.1102del XP_005247182.1:p.Val369Ter
NM_000097.7:c.1102del MANE Select NP_000088.3:p.Val369Ter
XM_005247125.4:c.1102del XP_005247182.1:p.Val369Ter
XR_001740025.2:n.1273del
XR_001740026.1:n.1837del
XR_001740027.1:n.1377del
XR_001740028.1:n.1343del