Canonical Allele Identifier: CA2511624
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98590717G>A , CM000665.2:g.98590717G>A GRCh38
NC_000003.11:g.98309561G>A , CM000665.1:g.98309561G>A GRCh37
NC_000003.10:g.99792251G>A NCBI36
NG_015994.1:g.7895C>T
NG_015994.2:g.7895C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.726C>T MANE Select ENSP00000497326.1:p.Gly242=
ENST00000264193.2:c.726C>T ENSP00000264193.2:p.Gly242=
ENST00000513674.1:c.*34-60C>T ENSP00000424924.1:n.*34-60C>T
ENST00000515041.1:n.832C>T
NM_000097.5:c.726C>T NP_000088.3:p.Gly242=
XM_005247125.3:c.726C>T XP_005247182.1:p.Gly242=
XM_011512437.1:c.726C>T XP_011510739.1:p.Gly242=
NM_000097.7:c.726C>T MANE Select NP_000088.3:p.Gly242=
XM_005247125.4:c.726C>T XP_005247182.1:p.Gly242=
XR_001740025.2:n.897C>T
XR_001740026.1:n.902C>T
XR_001740027.1:n.906C>T
XR_001740028.1:n.906C>T