Canonical Allele Identifier: CA353644975
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585523A>T , CM000665.2:g.98585523A>T GRCh38
NC_000003.11:g.98304367A>T , CM000665.1:g.98304367A>T GRCh37
NC_000003.10:g.99787057A>T NCBI36
NG_015994.1:g.13089T>A
NG_015994.2:g.13089T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1090T>A MANE Select ENSP00000497326.1:p.Ser364Thr
ENST00000264193.2:c.1090T>A ENSP00000264193.2:p.Ser364Thr
ENST00000510489.1:n.340T>A
NM_000097.5:c.1090T>A NP_000088.3:p.Ser364Thr
XM_005247125.3:c.1090T>A XP_005247182.1:p.Ser364Thr
NM_000097.7:c.1090T>A MANE Select NP_000088.3:p.Ser364Thr
XM_005247125.4:c.1090T>A XP_005247182.1:p.Ser364Thr
XR_001740025.2:n.1261T>A
XR_001740026.1:n.1825T>A
XR_001740027.1:n.1365T>A
XR_001740028.1:n.1331T>A