Canonical Allele Identifier: CA1387393825
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585703A= , CM000665.2:g.98585703A= GRCh38
NC_000003.11:g.98304547A= , CM000665.1:g.98304547A= GRCh37
NC_000003.10:g.99787237A= NCBI36
NG_015994.1:g.12909T=
NG_015994.2:g.12909T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-44T= MANE Select ENSP00000497326.1:n.954-44T=
ENST00000264193.2:c.954-44T= ENSP00000264193.2:n.954-44T=
ENST00000510489.1:n.160T=
NM_000097.5:c.954-44T= NP_000088.3:n.954-44T=
XM_005247125.3:c.954-44T= XP_005247182.1:n.954-44T=
NM_000097.7:c.954-44T= MANE Select NP_000088.3:n.954-44T=
XM_005247125.4:c.954-44T= XP_005247182.1:n.954-44T=
XR_001740025.2:n.1125-44T=
XR_001740026.1:n.1645T=
XR_001740027.1:n.1229-44T=
XR_001740028.1:n.1195-44T=