Canonical Allele Identifier: CA2511699

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98593036G>A , CM000665.2:g.98593036G>A	GRCh38
NC_000003.11:g.98311880G>A , CM000665.1:g.98311880G>A	GRCh37
NC_000003.10:g.99794570G>A	NCBI36
NG_015994.1:g.5576C>T
NG_015994.2:g.5576C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000097.7:c.469C>T MANE Select	NP_000088.3:p.Leu157=
ENST00000647941.2:c.469C>T MANE Select	ENSP00000497326.1:p.Leu157=
NM_000097.5:c.469C>T	NP_000088.3:p.Leu157=
ENST00000264193.2:c.469C>T	ENSP00000264193.2:p.Leu157=
ENST00000513674.1:c.469C>T	ENSP00000424924.1:p.Leu157=
ENST00000515041.1:n.575C>T
XM_005247125.3:c.469C>T	XP_005247182.1:p.Leu157=
XM_005247125.4:c.469C>T	XP_005247182.1:p.Leu157=
XM_011512437.1:c.469C>T	XP_011510739.1:p.Leu157=
XR_001740025.2:n.640C>T
XR_001740026.1:n.645C>T
XR_001740027.1:n.649C>T
XR_001740028.1:n.649C>T