Canonical Allele Identifier: CA1387393555
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585486G= , CM000665.2:g.98585486G= GRCh38
NC_000003.11:g.98304330G= , CM000665.1:g.98304330G= GRCh37
NC_000003.10:g.99787020G= NCBI36
NG_015994.1:g.13126C=
NG_015994.2:g.13126C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.13C=
ENST00000647941.2:c.1127C= MANE Select ENSP00000497326.1:p.Ser376=
ENST00000264193.2:c.1127C= ENSP00000264193.2:p.Ser376=
ENST00000510489.1:n.377C=
ENST00000512905.5:c.13C=
NM_000097.5:c.1127C= NP_000088.3:p.Ser376=
XM_005247125.3:c.1127C= XP_005247182.1:p.Ser376=
NM_000097.7:c.1127C= MANE Select NP_000088.3:p.Ser376=
XM_005247125.4:c.1127C= XP_005247182.1:p.Ser376=
XR_001740025.2:n.1298C=
XR_001740026.1:n.1862C=
XR_001740027.1:n.1402C=
XR_001740028.1:n.1368C=