Canonical Allele Identifier: CA434875517

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98593172A>G , CM000665.2:g.98593172A>G	GRCh38
NC_000003.11:g.98312016A>G , CM000665.1:g.98312016A>G	GRCh37
NC_000003.10:g.99794706A>G	NCBI36
NG_015994.1:g.5440T>C
NG_015994.2:g.5440T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.333T>C MANE Select	ENSP00000497326.1:p.Thr111=
ENST00000264193.2:c.333T>C	ENSP00000264193.2:p.Thr111=
ENST00000513674.1:c.333T>C	ENSP00000424924.1:p.Thr111=
ENST00000515041.1:n.439T>C
NM_000097.5:c.333T>C	NP_000088.3:p.Thr111=
XM_005247125.3:c.333T>C	XP_005247182.1:p.Thr111=
XM_011512437.1:c.333T>C	XP_011510739.1:p.Thr111=
NM_000097.7:c.333T>C MANE Select	NP_000088.3:p.Thr111=
XM_005247125.4:c.333T>C	XP_005247182.1:p.Thr111=
XR_001740025.2:n.504T>C
XR_001740026.1:n.509T>C
XR_001740027.1:n.513T>C
XR_001740028.1:n.513T>C