Canonical Allele Identifier: CA2666706655
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585605_98585606del , CM000665.2:g.98585605_98585606del GRCh38
NC_000003.11:g.98304449_98304450del , CM000665.1:g.98304449_98304450del GRCh37
NC_000003.10:g.99787139_99787140del NCBI36
NG_015994.1:g.13006_13007del
NG_015994.2:g.13006_13007del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1007_1008del MANE Select ENSP00000497326.1:p.Gly336AspfsTer4
ENST00000264193.2:c.1007_1008del ENSP00000264193.2:p.Gly336AspfsTer4
ENST00000510489.1:n.257_258del
NM_000097.5:c.1007_1008del NP_000088.3:p.Gly336AspfsTer4
XM_005247125.3:c.1007_1008del XP_005247182.1:p.Gly336AspfsTer4
NM_000097.7:c.1007_1008del MANE Select NP_000088.3:p.Gly336AspfsTer4
XM_005247125.4:c.1007_1008del XP_005247182.1:p.Gly336AspfsTer4
XR_001740025.2:n.1178_1179del
XR_001740026.1:n.1742_1743del
XR_001740027.1:n.1282_1283del
XR_001740028.1:n.1248_1249del