Canonical Allele Identifier: CA784183898

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98591086_98591088del , CM000665.2:g.98591086_98591088del	GRCh38
NC_000003.11:g.98309930_98309932del , CM000665.1:g.98309930_98309932del	GRCh37
NC_000003.10:g.99792620_99792622del	NCBI36
NG_015994.1:g.7528_7530del
NG_015994.2:g.7528_7530del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647941.2:c.628_630del MANE Select	ENSP00000497326.1:p.Val210del
ENST00000264193.2:c.628_630del	ENSP00000264193.2:p.Val210del
ENST00000513674.1:c.508-19_508-17del	ENSP00000424924.1:n.508-19_508-17del
ENST00000515041.1:n.734_736del
NM_000097.5:c.628_630del	NP_000088.3:p.Val210del
XM_005247125.3:c.628_630del	XP_005247182.1:p.Val210del
XM_011512437.1:c.628_630del	XP_011510739.1:p.Val210del
NM_000097.7:c.628_630del MANE Select	NP_000088.3:p.Val210del
XM_005247125.4:c.628_630del	XP_005247182.1:p.Val210del
XR_001740025.2:n.799_801del
XR_001740026.1:n.804_806del
XR_001740027.1:n.808_810del
XR_001740028.1:n.808_810del