Canonical Allele Identifier: CA2395402647

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078261G= , CM000684.2:g.18078261G=	GRCh38
NC_000022.10:g.18561027G= , CM000684.1:g.18561027G=	GRCh37
NC_000022.9:g.16941027G=	NCBI36
NG_008339.1:g.5342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-116G= MANE Select	ENSP00000382648.4:n.-116G=
ENST00000474897.6:c.-81-35G=	ENSP00000434235.2:n.-81-35G=
ENST00000329627.11:c.-81-35G=	ENSP00000331106.5:n.-81-35G=
ENST00000399744.7:c.-116G=	ENSP00000382648.3:n.-116G=
ENST00000474897.5:c.-116G=	ENSP00000434235.1:n.-116G=
ENST00000610387.4:c.-81-35G=	ENSP00000482091.1:n.-81-35G=
NM_001127649.2:c.-116G=	NP_001121121.1:n.-116G=
NM_001199319.1:c.-81-35G=	NP_001186248.1:n.-81-35G=
NM_017929.5:c.-81-35G=	NP_060399.1:n.-81-35G=
NM_001127649.3:c.-116G= MANE Select	NP_001121121.1:n.-116G=
NM_001199319.2:c.-81-35G=	NP_001186248.1:n.-81-35G=
NM_017929.6:c.-81-35G=	NP_060399.1:n.-81-35G=