Canonical Allele Identifier: CA353644995
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585534G>T , CM000665.2:g.98585534G>T GRCh38
NC_000003.11:g.98304378G>T , CM000665.1:g.98304378G>T GRCh37
NC_000003.10:g.99787068G>T NCBI36
NG_015994.1:g.13078C>A
NG_015994.2:g.13078C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.1079C>A MANE Select ENSP00000497326.1:p.Ala360Asp
ENST00000264193.2:c.1079C>A ENSP00000264193.2:p.Ala360Asp
ENST00000510489.1:n.329C>A
NM_000097.5:c.1079C>A NP_000088.3:p.Ala360Asp
XM_005247125.3:c.1079C>A XP_005247182.1:p.Ala360Asp
NM_000097.7:c.1079C>A MANE Select NP_000088.3:p.Ala360Asp
XM_005247125.4:c.1079C>A XP_005247182.1:p.Ala360Asp
XR_001740025.2:n.1250C>A
XR_001740026.1:n.1814C>A
XR_001740027.1:n.1354C>A
XR_001740028.1:n.1320C>A