Canonical Allele Identifier: CA434770529

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304287T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585443T>A , CM000665.2:g.98585443T>A	GRCh38
NC_000003.11:g.98304287T>A , CM000665.1:g.98304287T>A	GRCh37
NC_000003.10:g.99786977T>A	NCBI36
NG_015994.1:g.13169A>T
NG_015994.2:g.13169A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.56A>T
ENST00000647941.2:c.1170A>T MANE Select	ENSP00000497326.1:p.Gly390=
ENST00000264193.2:c.1170A>T	ENSP00000264193.2:p.Gly390=
ENST00000510489.1:n.420A>T
ENST00000512905.5:c.56A>T
NM_000097.5:c.1170A>T	NP_000088.3:p.Gly390=
XM_005247125.3:c.1170A>T	XP_005247182.1:p.Gly390=
NM_000097.7:c.1170A>T MANE Select	NP_000088.3:p.Gly390=
XM_005247125.4:c.1170A>T	XP_005247182.1:p.Gly390=
XR_001740025.2:n.1341A>T
XR_001740026.1:n.1905A>T
XR_001740027.1:n.1445A>T
XR_001740028.1:n.1411A>T