Canonical Allele Identifier: CA1387393847
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585712G= , CM000665.2:g.98585712G= GRCh38
NC_000003.11:g.98304556G= , CM000665.1:g.98304556G= GRCh37
NC_000003.10:g.99787246G= NCBI36
NG_015994.1:g.12900C=
NG_015994.2:g.12900C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.954-53C= MANE Select ENSP00000497326.1:n.954-53C=
ENST00000264193.2:c.954-53C= ENSP00000264193.2:n.954-53C=
ENST00000510489.1:n.151C=
NM_000097.5:c.954-53C= NP_000088.3:n.954-53C=
XM_005247125.3:c.954-53C= XP_005247182.1:n.954-53C=
NM_000097.7:c.954-53C= MANE Select NP_000088.3:n.954-53C=
XM_005247125.4:c.954-53C= XP_005247182.1:n.954-53C=
XR_001740025.2:n.1125-53C=
XR_001740026.1:n.1636C=
XR_001740027.1:n.1229-53C=
XR_001740028.1:n.1195-53C=