Canonical Allele Identifier: CA353645230
Gene: CPOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585644G>C , CM000665.2:g.98585644G>C GRCh38
NC_000003.11:g.98304488G>C , CM000665.1:g.98304488G>C GRCh37
NC_000003.10:g.99787178G>C NCBI36
NG_015994.1:g.12968C>G
NG_015994.2:g.12968C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647941.2:c.969C>G MANE Select ENSP00000497326.1:p.Phe323Leu
ENST00000264193.2:c.969C>G ENSP00000264193.2:p.Phe323Leu
ENST00000510489.1:n.219C>G
NM_000097.5:c.969C>G NP_000088.3:p.Phe323Leu
XM_005247125.3:c.969C>G XP_005247182.1:p.Phe323Leu
NM_000097.7:c.969C>G MANE Select NP_000088.3:p.Phe323Leu
XM_005247125.4:c.969C>G XP_005247182.1:p.Phe323Leu
XR_001740025.2:n.1140C>G
XR_001740026.1:n.1704C>G
XR_001740027.1:n.1244C>G
XR_001740028.1:n.1210C>G