Canonical Allele Identifier: CA1387393783
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585647G= , CM000665.2:g.98585647G= GRCh38
NC_000003.11:g.98304491G= , CM000665.1:g.98304491G= GRCh37
NC_000003.10:g.99787181G= NCBI36
NG_015994.1:g.12965C=
NG_015994.2:g.12965C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.966C= MANE Select ENSP00000497326.1:p.Tyr322=
ENST00000264193.2:c.966C= ENSP00000264193.2:p.Tyr322=
ENST00000510489.1:n.216C=
NM_000097.5:c.966C= NP_000088.3:p.Tyr322=
XM_005247125.3:c.966C= XP_005247182.1:p.Tyr322=
NM_000097.7:c.966C= MANE Select NP_000088.3:p.Tyr322=
XM_005247125.4:c.966C= XP_005247182.1:p.Tyr322=
XR_001740025.2:n.1137C=
XR_001740026.1:n.1701C=
XR_001740027.1:n.1241C=
XR_001740028.1:n.1207C=