Canonical Allele Identifier: CA353644965
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585519T>C , CM000665.2:g.98585519T>C GRCh38
NC_000003.11:g.98304363T>C , CM000665.1:g.98304363T>C GRCh37
NC_000003.10:g.99787053T>C NCBI36
NG_015994.1:g.13093A>G
NG_015994.2:g.13093A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1094A>G MANE Select ENSP00000497326.1:p.Tyr365Cys
ENST00000264193.2:c.1094A>G ENSP00000264193.2:p.Tyr365Cys
ENST00000510489.1:n.344A>G
NM_000097.5:c.1094A>G NP_000088.3:p.Tyr365Cys
XM_005247125.3:c.1094A>G XP_005247182.1:p.Tyr365Cys
NM_000097.7:c.1094A>G MANE Select NP_000088.3:p.Tyr365Cys
XM_005247125.4:c.1094A>G XP_005247182.1:p.Tyr365Cys
XR_001740025.2:n.1265A>G
XR_001740026.1:n.1829A>G
XR_001740027.1:n.1369A>G
XR_001740028.1:n.1335A>G