Canonical Allele Identifier: CA1387393524
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585474T= , CM000665.2:g.98585474T= GRCh38
NC_000003.11:g.98304318T= , CM000665.1:g.98304318T= GRCh37
NC_000003.10:g.99787008T= NCBI36
NG_015994.1:g.13138A=
NG_015994.2:g.13138A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.25A=
ENST00000647941.2:c.1139A= MANE Select ENSP00000497326.1:p.Gln380=
ENST00000264193.2:c.1139A= ENSP00000264193.2:p.Gln380=
ENST00000510489.1:n.389A=
ENST00000512905.5:c.25A=
NM_000097.5:c.1139A= NP_000088.3:p.Gln380=
XM_005247125.3:c.1139A= XP_005247182.1:p.Gln380=
NM_000097.7:c.1139A= MANE Select NP_000088.3:p.Gln380=
XM_005247125.4:c.1139A= XP_005247182.1:p.Gln380=
XR_001740025.2:n.1310A=
XR_001740026.1:n.1874A=
XR_001740027.1:n.1414A=
XR_001740028.1:n.1380A=