Canonical Allele Identifier: CA1387393865
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585741G= , CM000665.2:g.98585741G= GRCh38
NC_000003.11:g.98304585G= , CM000665.1:g.98304585G= GRCh37
NC_000003.10:g.99787275G= NCBI36
NG_015994.1:g.12871C=
NG_015994.2:g.12871C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-82C= MANE Select ENSP00000497326.1:n.954-82C=
ENST00000264193.2:c.954-82C= ENSP00000264193.2:n.954-82C=
ENST00000510489.1:n.122C=
NM_000097.5:c.954-82C= NP_000088.3:n.954-82C=
XM_005247125.3:c.954-82C= XP_005247182.1:n.954-82C=
NM_000097.7:c.954-82C= MANE Select NP_000088.3:n.954-82C=
XM_005247125.4:c.954-82C= XP_005247182.1:n.954-82C=
XR_001740025.2:n.1125-82C=
XR_001740026.1:n.1607C=
XR_001740027.1:n.1229-82C=
XR_001740028.1:n.1195-82C=