Canonical Allele Identifier: CA434770664

Gene: CPOX

Linked Data

• MyVariant Identifiers: chr3:g.98304371A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585527A>T , CM000665.2:g.98585527A>T	GRCh38
NC_000003.11:g.98304371A>T , CM000665.1:g.98304371A>T	GRCh37
NC_000003.10:g.99787061A>T	NCBI36
NG_015994.1:g.13085T>A
NG_015994.2:g.13085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1086T>A MANE Select	ENSP00000497326.1:p.Val362=
ENST00000264193.2:c.1086T>A	ENSP00000264193.2:p.Val362=
ENST00000510489.1:n.336T>A
NM_000097.5:c.1086T>A	NP_000088.3:p.Val362=
XM_005247125.3:c.1086T>A	XP_005247182.1:p.Val362=
NM_000097.7:c.1086T>A MANE Select	NP_000088.3:p.Val362=
XM_005247125.4:c.1086T>A	XP_005247182.1:p.Val362=
XR_001740025.2:n.1257T>A
XR_001740026.1:n.1821T>A
XR_001740027.1:n.1361T>A
XR_001740028.1:n.1327T>A