Canonical Allele Identifier: CA353644799

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304292T>A (hg19) ; chr3:g.98585448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585448T>A , CM000665.2:g.98585448T>A	GRCh38
NC_000003.11:g.98304292T>A , CM000665.1:g.98304292T>A	GRCh37
NC_000003.10:g.99786982T>A	NCBI36
NG_015994.1:g.13164A>T
NG_015994.2:g.13164A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.51A>T
ENST00000647941.2:c.1165A>T MANE Select	ENSP00000497326.1:p.Arg389Ter
ENST00000264193.2:c.1165A>T	ENSP00000264193.2:p.Arg389Ter
ENST00000510489.1:n.415A>T
ENST00000512905.5:c.51A>T
NM_000097.5:c.1165A>T	NP_000088.3:p.Arg389Ter
XM_005247125.3:c.1165A>T	XP_005247182.1:p.Arg389Ter
NM_000097.7:c.1165A>T MANE Select	NP_000088.3:p.Arg389Ter
XM_005247125.4:c.1165A>T	XP_005247182.1:p.Arg389Ter
XR_001740025.2:n.1336A>T
XR_001740026.1:n.1900A>T
XR_001740027.1:n.1440A>T
XR_001740028.1:n.1406A>T