Canonical Allele Identifier: CA353645003
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585538T>A , CM000665.2:g.98585538T>A GRCh38
NC_000003.11:g.98304382T>A , CM000665.1:g.98304382T>A GRCh37
NC_000003.10:g.99787072T>A NCBI36
NG_015994.1:g.13074A>T
NG_015994.2:g.13074A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.1075A>T MANE Select ENSP00000497326.1:p.Arg359Trp
ENST00000264193.2:c.1075A>T ENSP00000264193.2:p.Arg359Trp
ENST00000510489.1:n.325A>T
NM_000097.5:c.1075A>T NP_000088.3:p.Arg359Trp
XM_005247125.3:c.1075A>T XP_005247182.1:p.Arg359Trp
NM_000097.7:c.1075A>T MANE Select NP_000088.3:p.Arg359Trp
XM_005247125.4:c.1075A>T XP_005247182.1:p.Arg359Trp
XR_001740025.2:n.1246A>T
XR_001740026.1:n.1810A>T
XR_001740027.1:n.1350A>T
XR_001740028.1:n.1316A>T