Canonical Allele Identifier: CA2586965846
Gene: CPOX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585571_98585573dup , CM000665.2:g.98585571_98585573dup GRCh38
NC_000003.11:g.98304415_98304417dup , CM000665.1:g.98304415_98304417dup GRCh37
NC_000003.10:g.99787105_99787107dup NCBI36
NG_015994.1:g.13045_13047dup
NG_015994.2:g.13045_13047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1046_1048dup MANE Select ENSP00000497326.1:p.Glu349_Val350insGlu
ENST00000264193.2:c.1046_1048dup ENSP00000264193.2:p.Glu349_Val350insGlu
ENST00000510489.1:n.296_298dup
NM_000097.5:c.1046_1048dup NP_000088.3:p.Glu349_Val350insGlu
XM_005247125.3:c.1046_1048dup XP_005247182.1:p.Glu349_Val350insGlu
NM_000097.7:c.1046_1048dup MANE Select NP_000088.3:p.Glu349_Val350insGlu
XM_005247125.4:c.1046_1048dup XP_005247182.1:p.Glu349_Val350insGlu
XR_001740025.2:n.1217_1219dup
XR_001740026.1:n.1781_1783dup
XR_001740027.1:n.1321_1323dup
XR_001740028.1:n.1287_1289dup
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