Canonical Allele Identifier: CA2395402612

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078191G= , CM000684.2:g.18078191G=	GRCh38
NC_000022.10:g.18560957G= , CM000684.1:g.18560957G=	GRCh37
NC_000022.9:g.16940957G=	NCBI36
NG_008339.1:g.5272G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-186G= MANE Select	ENSP00000382648.4:n.-186G=
ENST00000474897.6:c.-81-105G=	ENSP00000434235.2:n.-81-105G=
ENST00000329627.11:c.-81-105G=	ENSP00000331106.5:n.-81-105G=
ENST00000399744.7:c.-186G=	ENSP00000382648.3:n.-186G=
ENST00000474897.5:c.-186G=	ENSP00000434235.1:n.-186G=
ENST00000610387.4:c.-81-105G=	ENSP00000482091.1:n.-81-105G=
NM_001127649.2:c.-186G=	NP_001121121.1:n.-186G=
NM_001199319.1:c.-81-105G=	NP_001186248.1:n.-81-105G=
NM_017929.5:c.-81-105G=	NP_060399.1:n.-81-105G=
NM_001127649.3:c.-186G= MANE Select	NP_001121121.1:n.-186G=
NM_001199319.2:c.-81-105G=	NP_001186248.1:n.-81-105G=
NM_017929.6:c.-81-105G=	NP_060399.1:n.-81-105G=