Canonical Allele Identifier: CA1387393637

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585558C= , CM000665.2:g.98585558C=	GRCh38
NC_000003.11:g.98304402C= , CM000665.1:g.98304402C=	GRCh37
NC_000003.10:g.99787092C=	NCBI36
NG_015994.1:g.13054G=
NG_015994.2:g.13054G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1055G= MANE Select	ENSP00000497326.1:p.Arg352=
ENST00000264193.2:c.1055G=	ENSP00000264193.2:p.Arg352=
ENST00000510489.1:n.305G=
NM_000097.5:c.1055G=	NP_000088.3:p.Arg352=
XM_005247125.3:c.1055G=	XP_005247182.1:p.Arg352=
NM_000097.7:c.1055G= MANE Select	NP_000088.3:p.Arg352=
XM_005247125.4:c.1055G=	XP_005247182.1:p.Arg352=
XR_001740025.2:n.1226G=
XR_001740026.1:n.1790G=
XR_001740027.1:n.1330G=
XR_001740028.1:n.1296G=