Canonical Allele Identifier: CA410267005

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18083435A>G , CM000684.2:g.18083435A>G	GRCh38
NC_000022.10:g.18566201A>G , CM000684.1:g.18566201A>G	GRCh37
NC_000022.9:g.16946201A>G	NCBI36
NG_008339.1:g.10516A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001127649.3:c.372-2A>G MANE Select	NP_001121121.1:n.372-2A>G
ENST00000399744.8:c.372-2A>G MANE Select	ENSP00000382648.4:n.372-2A>G
NM_001127649.2:c.372-2A>G	NP_001121121.1:n.372-2A>G
NM_001199319.1:c.372-2A>G	NP_001186248.1:n.372-2A>G
NM_001199319.2:c.372-2A>G	NP_001186248.1:n.372-2A>G
NM_017929.5:c.372-2A>G	NP_060399.1:n.372-2A>G
NM_017929.6:c.372-2A>G	NP_060399.1:n.372-2A>G
ENST00000329627.11:c.372-2A>G	ENSP00000331106.5:n.372-2A>G
ENST00000399744.7:c.372-2A>G	ENSP00000382648.3:n.372-2A>G
ENST00000428061.2:c.372-2A>G	ENSP00000412441.2:n.372-2A>G
ENST00000474897.5:c.371+3421A>G	ENSP00000434235.1:n.371+3421A>G
ENST00000474897.6:c.372-2A>G	ENSP00000434235.2:n.372-2A>G
ENST00000610387.4:c.372-2A>G	ENSP00000482091.1:n.372-2A>G