Canonical Allele Identifier: CA944417640

Gene: PEX5

Linked Data

• dbSNP Id: rs1945508305
• gnomAD v3: 12-7211017-AG-A
• gnomAD v4: 12-7211017-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7211022del , CM000674.2:g.7211022del	GRCh38
NC_000012.11:g.7363618del , CM000674.1:g.7363618del	GRCh37
NC_000012.10:g.7254885del	NCBI36
NG_008448.1:g.26860del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675855.1:c.*799del MANE Select	ENSP00000502374.1:n.*799del
ENST00000266563.9:c.*799del	ENSP00000266563.5:n.*799del
ENST00000266564.7:c.*799del	ENSP00000266564.3:n.*799del
ENST00000455147.6:c.*19+780del	ENSP00000400647.2:n.*19+780del
ENST00000541850.1:c.113+780del
NM_000319.4:c.*799del	NP_000310.2:n.*799del
NM_001131023.1:c.*799del	NP_001124495.1:n.*799del
NM_001131024.1:c.*799del	NP_001124496.1:n.*799del
NM_001131025.1:c.*799del	NP_001124497.1:n.*799del
NM_001131026.1:c.*19+780del	NP_001124498.1:n.*19+780del
NM_001300789.1:c.*799del	NP_001287718.1:n.*799del
XM_005253455.1:c.*799del	XP_005253512.1:n.*799del
XM_011520793.1:c.*799del	XP_011519095.1:n.*799del
XM_011520794.1:c.*19+780del	XP_011519096.1:n.*19+780del
XM_011520795.1:c.*799del	XP_011519097.1:n.*799del
XM_011520796.1:c.*799del	XP_011519098.1:n.*799del
XM_011520797.1:c.*799del	XP_011519099.1:n.*799del
XM_011520798.1:c.*799del	XP_011519100.1:n.*799del
XM_011520799.1:c.*799del	XP_011519101.1:n.*799del
XM_011520800.1:c.*799del	XP_011519102.1:n.*799del
XM_011520801.1:c.*799del	XP_011519103.1:n.*799del
XM_011520802.1:c.*799del	XP_011519104.1:n.*799del
NM_001351124.1:c.*799del	NP_001338053.1:n.*799del
NM_001351126.1:c.*799del	NP_001338055.1:n.*799del
NM_001351127.1:c.*799del	NP_001338056.1:n.*799del
NM_001351128.1:c.*799del	NP_001338057.1:n.*799del
NM_001351130.1:c.*799del	NP_001338059.1:n.*799del
NM_001351131.1:c.*799del	NP_001338060.1:n.*799del
NM_001351132.1:c.*799del	NP_001338061.1:n.*799del
NM_001351133.1:c.*799del	NP_001338062.1:n.*799del
NM_001351134.1:c.*799del	NP_001338063.1:n.*799del
NM_001351135.1:c.*799del	NP_001338064.1:n.*799del
NM_001351136.1:c.*799del	NP_001338065.1:n.*799del
NM_001351137.1:c.*799del	NP_001338066.1:n.*799del
NM_001351138.1:c.*799del	NP_001338067.1:n.*799del
NM_001351139.1:c.*799del	NP_001338068.1:n.*799del
NM_001351140.1:c.*799del	NP_001338069.1:n.*799del
XM_011520793.2:c.*799del	XP_011519095.1:n.*799del
XM_011520802.2:c.*799del	XP_011519104.1:n.*799del
XM_017019744.1:c.*799del	XP_016875233.1:n.*799del
XM_017019745.1:c.*19+780del	XP_016875234.1:n.*19+780del
XM_017019746.1:c.*799del	XP_016875235.1:n.*799del
XM_017019747.1:c.*799del	XP_016875236.1:n.*799del
XM_017019748.1:c.*799del	XP_016875237.1:n.*799del
XM_017019749.1:c.*19+780del	XP_016875238.1:n.*19+780del
XM_017019750.1:c.*799del	XP_016875239.1:n.*799del
XR_001748833.1:n.2425+780del
NM_000319.5:c.*799del	NP_000310.2:n.*799del
NM_001131023.2:c.*799del	NP_001124495.1:n.*799del
NM_001131024.2:c.*799del	NP_001124496.1:n.*799del
NM_001131025.2:c.*799del	NP_001124497.1:n.*799del
NM_001131026.2:c.*19+780del	NP_001124498.1:n.*19+780del
NM_001300789.3:c.*799del	NP_001287718.2:n.*799del
NM_001351124.3:c.*799del	NP_001338053.1:n.*799del
NM_001351126.2:c.*799del	NP_001338055.1:n.*799del
NM_001351127.2:c.*799del	NP_001338056.1:n.*799del
NM_001351128.2:c.*799del	NP_001338057.1:n.*799del
NM_001351130.3:c.*799del	NP_001338059.1:n.*799del
NM_001351131.2:c.*799del	NP_001338060.1:n.*799del
NM_001351132.2:c.*799del MANE Select	NP_001338061.1:n.*799del
NM_001351133.2:c.*799del	NP_001338062.1:n.*799del
NM_001351134.2:c.*799del	NP_001338063.1:n.*799del
NM_001351135.3:c.*799del	NP_001338064.2:n.*799del
NM_001351136.2:c.*799del	NP_001338065.1:n.*799del
NM_001351137.3:c.*799del	NP_001338066.2:n.*799del
NM_001351138.2:c.*799del	NP_001338067.1:n.*799del
NM_001351139.2:c.*799del	NP_001338068.1:n.*799del
NM_001351140.2:c.*799del	NP_001338069.1:n.*799del
NM_001374645.1:c.*799del	NP_001361574.1:n.*799del
NM_001374646.1:c.*19+780del	NP_001361575.1:n.*19+780del
NM_001374647.2:c.*799del	NP_001361576.1:n.*799del
NM_001374648.2:c.*799del	NP_001361577.1:n.*799del
NM_001374649.2:c.*799del	NP_001361578.1:n.*799del