Canonical Allele Identifier: CA434770612

Gene: CPOX

Linked Data

• COSMIC: COSM1178001
• MyVariant Identifiers: chr3:g.98304323G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585479G>T , CM000665.2:g.98585479G>T	GRCh38
NC_000003.11:g.98304323G>T , CM000665.1:g.98304323G>T	GRCh37
NC_000003.10:g.99787013G>T	NCBI36
NG_015994.1:g.13133C>A
NG_015994.2:g.13133C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.20C>A
ENST00000647941.2:c.1134C>A MANE Select	ENSP00000497326.1:p.Thr378=
ENST00000264193.2:c.1134C>A	ENSP00000264193.2:p.Thr378=
ENST00000510489.1:n.384C>A
ENST00000512905.5:c.20C>A
NM_000097.5:c.1134C>A	NP_000088.3:p.Thr378=
XM_005247125.3:c.1134C>A	XP_005247182.1:p.Thr378=
NM_000097.7:c.1134C>A MANE Select	NP_000088.3:p.Thr378=
XM_005247125.4:c.1134C>A	XP_005247182.1:p.Thr378=
XR_001740025.2:n.1305C>A
XR_001740026.1:n.1869C>A
XR_001740027.1:n.1409C>A
XR_001740028.1:n.1375C>A