Canonical Allele Identifier: CA353644849

Gene: CPOX

Linked Data

• gnomAD v4: 3-98585469-T-A
• MyVariant Identifiers: chr3:g.98304313T>A (hg19) ; chr3:g.98585469T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585469T>A , CM000665.2:g.98585469T>A	GRCh38
NC_000003.11:g.98304313T>A , CM000665.1:g.98304313T>A	GRCh37
NC_000003.10:g.99787003T>A	NCBI36
NG_015994.1:g.13143A>T
NG_015994.2:g.13143A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.30A>T
ENST00000647941.2:c.1144A>T MANE Select	ENSP00000497326.1:p.Lys382Ter
ENST00000264193.2:c.1144A>T	ENSP00000264193.2:p.Lys382Ter
ENST00000510489.1:n.394A>T
ENST00000512905.5:c.30A>T
NM_000097.5:c.1144A>T	NP_000088.3:p.Lys382Ter
XM_005247125.3:c.1144A>T	XP_005247182.1:p.Lys382Ter
NM_000097.7:c.1144A>T MANE Select	NP_000088.3:p.Lys382Ter
XM_005247125.4:c.1144A>T	XP_005247182.1:p.Lys382Ter
XR_001740025.2:n.1315A>T
XR_001740026.1:n.1879A>T
XR_001740027.1:n.1419A>T
XR_001740028.1:n.1385A>T