Canonical Allele Identifier: CA353644800

Gene: CPOX

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512905.6:c.51A>G
ENST00000647941.2:c.1165A>G MANE Select	ENSP00000497326.1:p.Arg389Gly
ENST00000264193.2:c.1165A>G	ENSP00000264193.2:p.Arg389Gly
ENST00000510489.1:n.415A>G
ENST00000512905.5:c.51A>G
NM_000097.5:c.1165A>G	NP_000088.3:p.Arg389Gly
XM_005247125.3:c.1165A>G	XP_005247182.1:p.Arg389Gly
NM_000097.7:c.1165A>G MANE Select	NP_000088.3:p.Arg389Gly
XM_005247125.4:c.1165A>G	XP_005247182.1:p.Arg389Gly
XR_001740025.2:n.1336A>G
XR_001740026.1:n.1900A>G
XR_001740027.1:n.1440A>G
XR_001740028.1:n.1406A>G