Canonical Allele Identifier: CA353645078
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585572C>A , CM000665.2:g.98585572C>A GRCh38
NC_000003.11:g.98304416C>A , CM000665.1:g.98304416C>A GRCh37
NC_000003.10:g.99787106C>A NCBI36
NG_015994.1:g.13040G>T
NG_015994.2:g.13040G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1041G>T MANE Select ENSP00000497326.1:p.Lys347Asn
ENST00000264193.2:c.1041G>T ENSP00000264193.2:p.Lys347Asn
ENST00000510489.1:n.291G>T
NM_000097.5:c.1041G>T NP_000088.3:p.Lys347Asn
XM_005247125.3:c.1041G>T XP_005247182.1:p.Lys347Asn
NM_000097.7:c.1041G>T MANE Select NP_000088.3:p.Lys347Asn
XM_005247125.4:c.1041G>T XP_005247182.1:p.Lys347Asn
XR_001740025.2:n.1212G>T
XR_001740026.1:n.1776G>T
XR_001740027.1:n.1316G>T
XR_001740028.1:n.1282G>T