Canonical Allele Identifier: CA2586965844
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585445_98585447del , CM000665.2:g.98585445_98585447del GRCh38
NC_000003.11:g.98304289_98304291del , CM000665.1:g.98304289_98304291del GRCh37
NC_000003.10:g.99786979_99786981del NCBI36
NG_015994.1:g.13167_13169del
NG_015994.2:g.13167_13169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.54_56del
ENST00000647941.2:c.1168_1170del MANE Select ENSP00000497326.1:p.Gly390del
ENST00000264193.2:c.1168_1170del ENSP00000264193.2:p.Gly390del
ENST00000510489.1:n.418_420del
ENST00000512905.5:c.54_56del
NM_000097.5:c.1168_1170del NP_000088.3:p.Gly390del
XM_005247125.3:c.1168_1170del XP_005247182.1:p.Gly390del
NM_000097.7:c.1168_1170del MANE Select NP_000088.3:p.Gly390del
XM_005247125.4:c.1168_1170del XP_005247182.1:p.Gly390del
XR_001740025.2:n.1339_1341del
XR_001740026.1:n.1903_1905del
XR_001740027.1:n.1443_1445del
XR_001740028.1:n.1409_1411del