Canonical Allele Identifier: CA1387393604
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585540G= , CM000665.2:g.98585540G= GRCh38
NC_000003.11:g.98304384G= , CM000665.1:g.98304384G= GRCh37
NC_000003.10:g.99787074G= NCBI36
NG_015994.1:g.13072C=
NG_015994.2:g.13072C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1073C= MANE Select ENSP00000497326.1:p.Ala358=
ENST00000264193.2:c.1073C= ENSP00000264193.2:p.Ala358=
ENST00000510489.1:n.323C=
NM_000097.5:c.1073C= NP_000088.3:p.Ala358=
XM_005247125.3:c.1073C= XP_005247182.1:p.Ala358=
NM_000097.7:c.1073C= MANE Select NP_000088.3:p.Ala358=
XM_005247125.4:c.1073C= XP_005247182.1:p.Ala358=
XR_001740025.2:n.1244C=
XR_001740026.1:n.1808C=
XR_001740027.1:n.1348C=
XR_001740028.1:n.1314C=