Canonical Allele Identifier: CA2395403479

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18079974C= , CM000684.2:g.18079974C=	GRCh38
NC_000022.10:g.18562740C= , CM000684.1:g.18562740C=	GRCh37
NC_000022.9:g.16942740C=	NCBI36
NG_008339.1:g.7055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.331C= MANE Select	ENSP00000382648.4:p.Gln111=
ENST00000474897.6:c.331C=	ENSP00000434235.2:p.Gln111=
ENST00000329627.11:c.331C=	ENSP00000331106.5:p.Gln111=
ENST00000399744.7:c.331C=	ENSP00000382648.3:p.Gln111=
ENST00000428061.2:c.331C=	ENSP00000412441.2:p.Gln111=
ENST00000474897.5:c.331C=	ENSP00000434235.1:p.Gln111=
ENST00000610387.4:c.331C=	ENSP00000482091.1:p.Gln111=
NM_001127649.2:c.331C=	NP_001121121.1:p.Gln111=
NM_001199319.1:c.331C=	NP_001186248.1:p.Gln111=
NM_017929.5:c.331C=	NP_060399.1:p.Gln111=
NM_001127649.3:c.331C= MANE Select	NP_001121121.1:p.Gln111=
NM_001199319.2:c.331C=	NP_001186248.1:p.Gln111=
NM_017929.6:c.331C=	NP_060399.1:p.Gln111=