Canonical Allele Identifier: CA1051334576

Gene: CPOX

Linked Data

• gnomAD v3: 3-98585607-C-CG
• gnomAD v4: 3-98585607-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98585607_98585608insG , CM000665.2:g.98585607_98585608insG	GRCh38
NC_000003.11:g.98304451_98304452insG , CM000665.1:g.98304451_98304452insG	GRCh37
NC_000003.10:g.99787141_99787142insG	NCBI36
NG_015994.1:g.13004_13005insC
NG_015994.2:g.13004_13005insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.1005_1006insC MANE Select	ENSP00000497326.1:p.Gly336ArgfsTer5
ENST00000264193.2:c.1005_1006insC	ENSP00000264193.2:p.Gly336ArgfsTer5
ENST00000510489.1:n.255_256insC
NM_000097.5:c.1005_1006insC	NP_000088.3:p.Gly336ArgfsTer5
XM_005247125.3:c.1005_1006insC	XP_005247182.1:p.Gly336ArgfsTer5
NM_000097.7:c.1005_1006insC MANE Select	NP_000088.3:p.Gly336ArgfsTer5
XM_005247125.4:c.1005_1006insC	XP_005247182.1:p.Gly336ArgfsTer5
XR_001740025.2:n.1176_1177insC
XR_001740026.1:n.1740_1741insC
XR_001740027.1:n.1280_1281insC
XR_001740028.1:n.1246_1247insC