Canonical Allele Identifier: CA2395402659

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078279T= , CM000684.2:g.18078279T=	GRCh38
NC_000022.10:g.18561045T= , CM000684.1:g.18561045T=	GRCh37
NC_000022.9:g.16941045T=	NCBI36
NG_008339.1:g.5360T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-98T= MANE Select	ENSP00000382648.4:n.-98T=
ENST00000474897.6:c.-81-17T=	ENSP00000434235.2:n.-81-17T=
ENST00000329627.11:c.-81-17T=	ENSP00000331106.5:n.-81-17T=
ENST00000399744.7:c.-98T=	ENSP00000382648.3:n.-98T=
ENST00000474897.5:c.-98T=	ENSP00000434235.1:n.-98T=
ENST00000610387.4:c.-81-17T=	ENSP00000482091.1:n.-81-17T=
NM_001127649.2:c.-98T=	NP_001121121.1:n.-98T=
NM_001199319.1:c.-81-17T=	NP_001186248.1:n.-81-17T=
NM_017929.5:c.-81-17T=	NP_060399.1:n.-81-17T=
NM_001127649.3:c.-98T= MANE Select	NP_001121121.1:n.-98T=
NM_001199319.2:c.-81-17T=	NP_001186248.1:n.-81-17T=
NM_017929.6:c.-81-17T=	NP_060399.1:n.-81-17T=