Canonical Allele Identifier: CA1387393588

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585530T= , CM000665.2:g.98585530T=	GRCh38
NC_000003.11:g.98304374T= , CM000665.1:g.98304374T=	GRCh37
NC_000003.10:g.99787064T=	NCBI36
NG_015994.1:g.13082A=
NG_015994.2:g.13082A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1083A= MANE Select	ENSP00000497326.1:p.Val361=
ENST00000264193.2:c.1083A=	ENSP00000264193.2:p.Val361=
ENST00000510489.1:n.333A=
NM_000097.5:c.1083A=	NP_000088.3:p.Val361=
XM_005247125.3:c.1083A=	XP_005247182.1:p.Val361=
NM_000097.7:c.1083A= MANE Select	NP_000088.3:p.Val361=
XM_005247125.4:c.1083A=	XP_005247182.1:p.Val361=
XR_001740025.2:n.1254A=
XR_001740026.1:n.1818A=
XR_001740027.1:n.1358A=
XR_001740028.1:n.1324A=