Canonical Allele Identifier: CA1387393598
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585535C= , CM000665.2:g.98585535C= GRCh38
NC_000003.11:g.98304379C= , CM000665.1:g.98304379C= GRCh37
NC_000003.10:g.99787069C= NCBI36
NG_015994.1:g.13077G=
NG_015994.2:g.13077G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.1078G= MANE Select ENSP00000497326.1:p.Ala360=
ENST00000264193.2:c.1078G= ENSP00000264193.2:p.Ala360=
ENST00000510489.1:n.328G=
NM_000097.5:c.1078G= NP_000088.3:p.Ala360=
XM_005247125.3:c.1078G= XP_005247182.1:p.Ala360=
NM_000097.7:c.1078G= MANE Select NP_000088.3:p.Ala360=
XM_005247125.4:c.1078G= XP_005247182.1:p.Ala360=
XR_001740025.2:n.1249G=
XR_001740026.1:n.1813G=
XR_001740027.1:n.1353G=
XR_001740028.1:n.1319G=