Canonical Allele Identifier: CA1387393656
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585568C= , CM000665.2:g.98585568C= GRCh38
NC_000003.11:g.98304412C= , CM000665.1:g.98304412C= GRCh37
NC_000003.10:g.99787102C= NCBI36
NG_015994.1:g.13044G=
NG_015994.2:g.13044G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1045G= MANE Select ENSP00000497326.1:p.Glu349=
ENST00000264193.2:c.1045G= ENSP00000264193.2:p.Glu349=
ENST00000510489.1:n.295G=
NM_000097.5:c.1045G= NP_000088.3:p.Glu349=
XM_005247125.3:c.1045G= XP_005247182.1:p.Glu349=
NM_000097.7:c.1045G= MANE Select NP_000088.3:p.Glu349=
XM_005247125.4:c.1045G= XP_005247182.1:p.Glu349=
XR_001740025.2:n.1216G=
XR_001740026.1:n.1780G=
XR_001740027.1:n.1320G=
XR_001740028.1:n.1286G=