Canonical Allele Identifier: CA1387393845
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585711T= , CM000665.2:g.98585711T= GRCh38
NC_000003.11:g.98304555T= , CM000665.1:g.98304555T= GRCh37
NC_000003.10:g.99787245T= NCBI36
NG_015994.1:g.12901A=
NG_015994.2:g.12901A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-52A= MANE Select ENSP00000497326.1:n.954-52A=
ENST00000264193.2:c.954-52A= ENSP00000264193.2:n.954-52A=
ENST00000510489.1:n.152A=
NM_000097.5:c.954-52A= NP_000088.3:n.954-52A=
XM_005247125.3:c.954-52A= XP_005247182.1:n.954-52A=
NM_000097.7:c.954-52A= MANE Select NP_000088.3:n.954-52A=
XM_005247125.4:c.954-52A= XP_005247182.1:n.954-52A=
XR_001740025.2:n.1125-52A=
XR_001740026.1:n.1637A=
XR_001740027.1:n.1229-52A=
XR_001740028.1:n.1195-52A=