Canonical Allele Identifier: CA1387393646

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585560A= , CM000665.2:g.98585560A=	GRCh38
NC_000003.11:g.98304404A= , CM000665.1:g.98304404A=	GRCh37
NC_000003.10:g.99787094A=	NCBI36
NG_015994.1:g.13052T=
NG_015994.2:g.13052T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1053T= MANE Select	ENSP00000497326.1:p.Phe351=
ENST00000264193.2:c.1053T=	ENSP00000264193.2:p.Phe351=
ENST00000510489.1:n.303T=
NM_000097.5:c.1053T=	NP_000088.3:p.Phe351=
XM_005247125.3:c.1053T=	XP_005247182.1:p.Phe351=
NM_000097.7:c.1053T= MANE Select	NP_000088.3:p.Phe351=
XM_005247125.4:c.1053T=	XP_005247182.1:p.Phe351=
XR_001740025.2:n.1224T=
XR_001740026.1:n.1788T=
XR_001740027.1:n.1328T=
XR_001740028.1:n.1294T=