Canonical Allele Identifier: CA2395402807

Gene: PEX26

Linked Data

• dbSNP Id: rs1926399395

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078515_18078517del , CM000684.2:g.18078515_18078517del	GRCh38
NC_000022.10:g.18561281_18561283del , CM000684.1:g.18561281_18561283del	GRCh37
NC_000022.9:g.16941281_16941283del	NCBI36
NG_008339.1:g.5596_5598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.139_141del MANE Select	ENSP00000382648.4:p.Val47del
ENST00000474897.6:c.139_141del	ENSP00000434235.2:p.Val47del
ENST00000329627.11:c.139_141del	ENSP00000331106.5:p.Val47del
ENST00000399744.7:c.139_141del	ENSP00000382648.3:p.Val47del
ENST00000428061.2:c.139_141del	ENSP00000412441.2:p.Val47del
ENST00000474897.5:c.139_141del	ENSP00000434235.1:p.Val47del
ENST00000610387.4:c.139_141del	ENSP00000482091.1:p.Val47del
NM_001127649.2:c.139_141del	NP_001121121.1:p.Val47del
NM_001199319.1:c.139_141del	NP_001186248.1:p.Val47del
NM_017929.5:c.139_141del	NP_060399.1:p.Val47del
NM_001127649.3:c.139_141del MANE Select	NP_001121121.1:p.Val47del
NM_001199319.2:c.139_141del	NP_001186248.1:p.Val47del
NM_017929.6:c.139_141del	NP_060399.1:p.Val47del