Canonical Allele Identifier: CA2580611963

Gene: CPOX

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98592996_98593017delinsCCAGAATCAGCAGCT , CM000665.2:g.98592996_98593017delinsCCAGAATCAGCAGCT	GRCh38
NC_000003.11:g.98311840_98311861delinsCCAGAATCAGCAGCT , CM000665.1:g.98311840_98311861delinsCCAGAATCAGCAGCT	GRCh37
NC_000003.10:g.99794530_99794551delinsCCAGAATCAGCAGCT	NCBI36
NG_015994.1:g.5595_5616delinsAGCTGCTGATTCTGG
NG_015994.2:g.5595_5616delinsAGCTGCTGATTCTGG

Transcript Alleles

HGVS	Amino-acid Change
NM_000097.7:c.488_509delinsAGCTGCTGATTCTGG MANE Select	NP_000088.3:p.Val163GlufsTer?
ENST00000647941.2:c.488_509delinsAGCTGCTGATTCTGG MANE Select	ENSP00000497326.1:p.Val163GlufsTer?
NM_000097.5:c.488_509delinsAGCTGCTGATTCTGG	NP_000088.3:p.Val163GlufsTer?
ENST00000264193.2:c.488_509delinsAGCTGCTGATTCTGG	ENSP00000264193.2:p.Val163GlufsTer?
ENST00000513674.1:c.488_507+2delinsAGCTGCTGATTCTGG
ENST00000515041.1:n.594_615delinsAGCTGCTGATTCTGG
XM_005247125.3:c.488_509delinsAGCTGCTGATTCTGG	XP_005247182.1:p.Val163GlufsTer?
XM_005247125.4:c.488_509delinsAGCTGCTGATTCTGG	XP_005247182.1:p.Val163GlufsTer?
XM_011512437.1:c.488_509delinsAGCTGCTGATTCTGG	XP_011510739.1:p.Val163GlufsTer?
XR_001740025.2:n.659_680delinsAGCTGCTGATTCTGG
XR_001740026.1:n.664_685delinsAGCTGCTGATTCTGG
XR_001740027.1:n.668_689delinsAGCTGCTGATTCTGG
XR_001740028.1:n.668_689delinsAGCTGCTGATTCTGG