Canonical Allele Identifier: CA916961978
Gene: CPOX HGNC NCBI

Linked Data

dbSNP Id: rs1576300550
gnomAD v4: 3-98585559-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585562dup , CM000665.2:g.98585562dup GRCh38
NC_000003.11:g.98304406dup , CM000665.1:g.98304406dup GRCh37
NC_000003.10:g.99787096dup NCBI36
NG_015994.1:g.13052dup
NG_015994.2:g.13052dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1053dup MANE Select ENSP00000497326.1:p.Arg352SerfsTer23
ENST00000264193.2:c.1053dup ENSP00000264193.2:p.Arg352SerfsTer23
ENST00000510489.1:n.303dup
NM_000097.5:c.1053dup NP_000088.3:p.Arg352SerfsTer23
XM_005247125.3:c.1053dup XP_005247182.1:p.Arg352SerfsTer23
NM_000097.7:c.1053dup MANE Select NP_000088.3:p.Arg352SerfsTer23
XM_005247125.4:c.1053dup XP_005247182.1:p.Arg352SerfsTer23
XR_001740025.2:n.1224dup
XR_001740026.1:n.1788dup
XR_001740027.1:n.1328dup
XR_001740028.1:n.1294dup
Search 100 bp 5'
Search 100 bp 3'