Canonical Allele Identifier: CA1387393779
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585643A= , CM000665.2:g.98585643A= GRCh38
NC_000003.11:g.98304487A= , CM000665.1:g.98304487A= GRCh37
NC_000003.10:g.99787177A= NCBI36
NG_015994.1:g.12969T=
NG_015994.2:g.12969T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.970T= MANE Select ENSP00000497326.1:p.Phe324=
ENST00000264193.2:c.970T= ENSP00000264193.2:p.Phe324=
ENST00000510489.1:n.220T=
NM_000097.5:c.970T= NP_000088.3:p.Phe324=
XM_005247125.3:c.970T= XP_005247182.1:p.Phe324=
NM_000097.7:c.970T= MANE Select NP_000088.3:p.Phe324=
XM_005247125.4:c.970T= XP_005247182.1:p.Phe324=
XR_001740025.2:n.1141T=
XR_001740026.1:n.1705T=
XR_001740027.1:n.1245T=
XR_001740028.1:n.1211T=