Canonical Allele Identifier: CA410267582

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18083533T>A , CM000684.2:g.18083533T>A	GRCh38
NC_000022.10:g.18566299T>A , CM000684.1:g.18566299T>A	GRCh37
NC_000022.9:g.16946299T>A	NCBI36
NG_008339.1:g.10614T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001127649.3:c.468T>A MANE Select	NP_001121121.1:p.Tyr156Ter
ENST00000399744.8:c.468T>A MANE Select	ENSP00000382648.4:p.Tyr156Ter
NM_001127649.2:c.468T>A	NP_001121121.1:p.Tyr156Ter
NM_001199319.1:c.468T>A	NP_001186248.1:p.Tyr156Ter
NM_001199319.2:c.468T>A	NP_001186248.1:p.Tyr156Ter
NM_017929.5:c.468T>A	NP_060399.1:p.Tyr156Ter
NM_017929.6:c.468T>A	NP_060399.1:p.Tyr156Ter
ENST00000329627.11:c.468T>A	ENSP00000331106.5:p.Tyr156Ter
ENST00000399744.7:c.468T>A	ENSP00000382648.3:p.Tyr156Ter
ENST00000428061.2:c.468T>A	ENSP00000412441.2:p.Tyr156Ter
ENST00000474897.5:c.371+3519T>A	ENSP00000434235.1:n.371+3519T>A
ENST00000474897.6:c.468T>A	ENSP00000434235.2:p.Tyr156Ter
ENST00000610387.4:c.468T>A	ENSP00000482091.1:p.Tyr156Ter