Canonical Allele Identifier: CA1387393346
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585285C= , CM000665.2:g.98585285C= GRCh38
NC_000003.11:g.98304129C= , CM000665.1:g.98304129C= GRCh37
NC_000003.10:g.99786819C= NCBI36
NG_015994.1:g.13327G=
NG_015994.2:g.13327G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000512905.6:c.58+156G=
ENST00000647941.2:c.1172+156G= MANE Select ENSP00000497326.1:n.1172+156G=
ENST00000264193.2:c.1172+156G= ENSP00000264193.2:n.1172+156G=
ENST00000510489.1:n.422+156G=
ENST00000512905.5:c.58+156G=
NM_000097.5:c.1172+156G= NP_000088.3:n.1172+156G=
XM_005247125.3:c.1172+156G= XP_005247182.1:n.1172+156G=
NM_000097.7:c.1172+156G= MANE Select NP_000088.3:n.1172+156G=
XM_005247125.4:c.1172+156G= XP_005247182.1:n.1172+156G=
XR_001740025.2:n.1343+156G=
XR_001740026.1:n.1907+156G=
XR_001740027.1:n.1447+156G=
XR_001740028.1:n.1413+156G=