Canonical Allele Identifier: CA2511626
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98590726A>T , CM000665.2:g.98590726A>T GRCh38
NC_000003.11:g.98309570A>T , CM000665.1:g.98309570A>T GRCh37
NC_000003.10:g.99792260A>T NCBI36
NG_015994.1:g.7886T>A
NG_015994.2:g.7886T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.717T>A MANE Select ENSP00000497326.1:p.Cys239Ter
ENST00000264193.2:c.717T>A ENSP00000264193.2:p.Cys239Ter
ENST00000513674.1:c.*34-69T>A ENSP00000424924.1:n.*34-69T>A
ENST00000515041.1:n.823T>A
NM_000097.5:c.717T>A NP_000088.3:p.Cys239Ter
XM_005247125.3:c.717T>A XP_005247182.1:p.Cys239Ter
XM_011512437.1:c.717T>A XP_011510739.1:p.Cys239Ter
NM_000097.7:c.717T>A MANE Select NP_000088.3:p.Cys239Ter
XM_005247125.4:c.717T>A XP_005247182.1:p.Cys239Ter
XR_001740025.2:n.888T>A
XR_001740026.1:n.893T>A
XR_001740027.1:n.897T>A
XR_001740028.1:n.897T>A