Canonical Allele Identifier: CA353644951
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585513G>C , CM000665.2:g.98585513G>C GRCh38
NC_000003.11:g.98304357G>C , CM000665.1:g.98304357G>C GRCh37
NC_000003.10:g.99787047G>C NCBI36
NG_015994.1:g.13099C>G
NG_015994.2:g.13099C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1100C>G MANE Select ENSP00000497326.1:p.Pro367Arg
ENST00000264193.2:c.1100C>G ENSP00000264193.2:p.Pro367Arg
ENST00000510489.1:n.350C>G
NM_000097.5:c.1100C>G NP_000088.3:p.Pro367Arg
XM_005247125.3:c.1100C>G XP_005247182.1:p.Pro367Arg
NM_000097.7:c.1100C>G MANE Select NP_000088.3:p.Pro367Arg
XM_005247125.4:c.1100C>G XP_005247182.1:p.Pro367Arg
XR_001740025.2:n.1271C>G
XR_001740026.1:n.1835C>G
XR_001740027.1:n.1375C>G
XR_001740028.1:n.1341C>G