Canonical Allele Identifier: CA2577832753
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585601del , CM000665.2:g.98585601del GRCh38
NC_000003.11:g.98304445del , CM000665.1:g.98304445del GRCh37
NC_000003.10:g.99787135del NCBI36
NG_015994.1:g.13016del
NG_015994.2:g.13016del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1017del MANE Select ENSP00000497326.1:p.Phe339LeufsTer23
ENST00000264193.2:c.1017del ENSP00000264193.2:p.Phe339LeufsTer23
ENST00000510489.1:n.267del
NM_000097.5:c.1017del NP_000088.3:p.Phe339LeufsTer23
XM_005247125.3:c.1017del XP_005247182.1:p.Phe339LeufsTer23
NM_000097.7:c.1017del MANE Select NP_000088.3:p.Phe339LeufsTer23
XM_005247125.4:c.1017del XP_005247182.1:p.Phe339LeufsTer23
XR_001740025.2:n.1188del
XR_001740026.1:n.1752del
XR_001740027.1:n.1292del
XR_001740028.1:n.1258del