Canonical Allele Identifier: CA353645049
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585560A>C , CM000665.2:g.98585560A>C GRCh38
NC_000003.11:g.98304404A>C , CM000665.1:g.98304404A>C GRCh37
NC_000003.10:g.99787094A>C NCBI36
NG_015994.1:g.13052T>G
NG_015994.2:g.13052T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1053T>G MANE Select ENSP00000497326.1:p.Phe351Leu
ENST00000264193.2:c.1053T>G ENSP00000264193.2:p.Phe351Leu
ENST00000510489.1:n.303T>G
NM_000097.5:c.1053T>G NP_000088.3:p.Phe351Leu
XM_005247125.3:c.1053T>G XP_005247182.1:p.Phe351Leu
NM_000097.7:c.1053T>G MANE Select NP_000088.3:p.Phe351Leu
XM_005247125.4:c.1053T>G XP_005247182.1:p.Phe351Leu
XR_001740025.2:n.1224T>G
XR_001740026.1:n.1788T>G
XR_001740027.1:n.1328T>G
XR_001740028.1:n.1294T>G