Canonical Allele Identifier: CA2511663
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98591100C>T , CM000665.2:g.98591100C>T GRCh38
NC_000003.11:g.98309944C>T , CM000665.1:g.98309944C>T GRCh37
NC_000003.10:g.99792634C>T NCBI36
NG_015994.1:g.7512G>A
NG_015994.2:g.7512G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.612G>A MANE Select ENSP00000497326.1:p.Gly204=
ENST00000264193.2:c.612G>A ENSP00000264193.2:p.Gly204=
ENST00000513674.1:c.508-35G>A ENSP00000424924.1:n.508-35G>A
ENST00000515041.1:n.718G>A
NM_000097.5:c.612G>A NP_000088.3:p.Gly204=
XM_005247125.3:c.612G>A XP_005247182.1:p.Gly204=
XM_011512437.1:c.612G>A XP_011510739.1:p.Gly204=
NM_000097.7:c.612G>A MANE Select NP_000088.3:p.Gly204=
XM_005247125.4:c.612G>A XP_005247182.1:p.Gly204=
XR_001740025.2:n.783G>A
XR_001740026.1:n.788G>A
XR_001740027.1:n.792G>A
XR_001740028.1:n.792G>A