Canonical Allele Identifier: CA410264008

Gene: PEX26

Linked Data

• MyVariant Identifiers: chr22:g.18561153A>T (hg19) ; chr22:g.18078387A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078387A>T , CM000684.2:g.18078387A>T	GRCh38
NC_000022.10:g.18561153A>T , CM000684.1:g.18561153A>T	GRCh37
NC_000022.9:g.16941153A>T	NCBI36
NG_008339.1:g.5468A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.11A>T MANE Select	ENSP00000382648.4:p.Asp4Val
ENST00000474897.6:c.11A>T	ENSP00000434235.2:p.Asp4Val
ENST00000329627.11:c.11A>T	ENSP00000331106.5:p.Asp4Val
ENST00000399744.7:c.11A>T	ENSP00000382648.3:p.Asp4Val
ENST00000428061.2:c.11A>T	ENSP00000412441.2:p.Asp4Val
ENST00000474897.5:c.11A>T	ENSP00000434235.1:p.Asp4Val
ENST00000610387.4:c.11A>T	ENSP00000482091.1:p.Asp4Val
NM_001127649.2:c.11A>T	NP_001121121.1:p.Asp4Val
NM_001199319.1:c.11A>T	NP_001186248.1:p.Asp4Val
NM_017929.5:c.11A>T	NP_060399.1:p.Asp4Val
NM_001127649.3:c.11A>T MANE Select	NP_001121121.1:p.Asp4Val
NM_001199319.2:c.11A>T	NP_001186248.1:p.Asp4Val
NM_017929.6:c.11A>T	NP_060399.1:p.Asp4Val