Canonical Allele Identifier: CA2666706654
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585523_98585525del , CM000665.2:g.98585523_98585525del GRCh38
NC_000003.11:g.98304367_98304369del , CM000665.1:g.98304367_98304369del GRCh37
NC_000003.10:g.99787057_99787059del NCBI36
NG_015994.1:g.13090_13092del
NG_015994.2:g.13090_13092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1091_1093del MANE Select ENSP00000497326.1:p.Ser364del
ENST00000264193.2:c.1091_1093del ENSP00000264193.2:p.Ser364del
ENST00000510489.1:n.341_343del
NM_000097.5:c.1091_1093del NP_000088.3:p.Ser364del
XM_005247125.3:c.1091_1093del XP_005247182.1:p.Ser364del
NM_000097.7:c.1091_1093del MANE Select NP_000088.3:p.Ser364del
XM_005247125.4:c.1091_1093del XP_005247182.1:p.Ser364del
XR_001740025.2:n.1262_1264del
XR_001740026.1:n.1826_1828del
XR_001740027.1:n.1366_1368del
XR_001740028.1:n.1332_1334del