Canonical Allele Identifier: CA353646385

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98593027G>A , CM000665.2:g.98593027G>A	GRCh38
NC_000003.11:g.98311871G>A , CM000665.1:g.98311871G>A	GRCh37
NC_000003.10:g.99794561G>A	NCBI36
NG_015994.1:g.5585C>T
NG_015994.2:g.5585C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000097.7:c.478C>T MANE Select	NP_000088.3:p.Gln160Ter
ENST00000647941.2:c.478C>T MANE Select	ENSP00000497326.1:p.Gln160Ter
NM_000097.5:c.478C>T	NP_000088.3:p.Gln160Ter
ENST00000264193.2:c.478C>T	ENSP00000264193.2:p.Gln160Ter
ENST00000513674.1:c.478C>T	ENSP00000424924.1:p.Gln160Ter
ENST00000515041.1:n.584C>T
XM_005247125.3:c.478C>T	XP_005247182.1:p.Gln160Ter
XM_005247125.4:c.478C>T	XP_005247182.1:p.Gln160Ter
XM_011512437.1:c.478C>T	XP_011510739.1:p.Gln160Ter
XR_001740025.2:n.649C>T
XR_001740026.1:n.654C>T
XR_001740027.1:n.658C>T
XR_001740028.1:n.658C>T