Canonical Allele Identifier: CA212740
Gene: CPOX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98593001_98593021del , CM000665.2:g.98593001_98593021del GRCh38
NC_000003.11:g.98311845_98311865del , CM000665.1:g.98311845_98311865del GRCh37
NC_000003.10:g.99794535_99794555del NCBI36
NG_015994.1:g.5596_5616del
NG_015994.2:g.5596_5616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.489_509del MANE Select ENSP00000497326.1:p.Cys164_Val170del
ENST00000264193.2:c.489_509del ENSP00000264193.2:p.Cys164_Val170del
ENST00000513674.1:c.489_507+2del
ENST00000515041.1:n.595_615del
NM_000097.5:c.489_509del NP_000088.3:p.Cys164_Val170del
XM_005247125.3:c.489_509del XP_005247182.1:p.Cys164_Val170del
XM_011512437.1:c.489_509del XP_011510739.1:p.Cys164_Val170del
NM_000097.7:c.489_509del MANE Select NP_000088.3:p.Cys164_Val170del
XM_005247125.4:c.489_509del XP_005247182.1:p.Cys164_Val170del
XR_001740025.2:n.660_680del
XR_001740026.1:n.665_685del
XR_001740027.1:n.669_689del
XR_001740028.1:n.669_689del
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