Canonical Allele Identifier: CA1387393575
Gene: CPOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98585510A= , CM000665.2:g.98585510A= GRCh38
NC_000003.11:g.98304354A= , CM000665.1:g.98304354A= GRCh37
NC_000003.10:g.99787044A= NCBI36
NG_015994.1:g.13102T=
NG_015994.2:g.13102T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647941.2:c.1103T= MANE Select ENSP00000497326.1:p.Leu368=
ENST00000264193.2:c.1103T= ENSP00000264193.2:p.Leu368=
ENST00000510489.1:n.353T=
NM_000097.5:c.1103T= NP_000088.3:p.Leu368=
XM_005247125.3:c.1103T= XP_005247182.1:p.Leu368=
NM_000097.7:c.1103T= MANE Select NP_000088.3:p.Leu368=
XM_005247125.4:c.1103T= XP_005247182.1:p.Leu368=
XR_001740025.2:n.1274T=
XR_001740026.1:n.1838T=
XR_001740027.1:n.1378T=
XR_001740028.1:n.1344T=