Canonical Allele Identifier: CA10093243
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 288461
dbSNP Id: rs201884779

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078576A>G , CM000684.2:g.18078576A>G GRCh38
NC_000022.10:g.18561342A>G , CM000684.1:g.18561342A>G GRCh37
NC_000022.9:g.16941342A>G NCBI36
NG_008339.1:g.5657A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.200A>G MANE Select ENSP00000382648.4:p.Asn67Ser
ENST00000474897.6:c.200A>G ENSP00000434235.2:p.Asn67Ser
ENST00000329627.11:c.200A>G ENSP00000331106.5:p.Asn67Ser
ENST00000399744.7:c.200A>G ENSP00000382648.3:p.Asn67Ser
ENST00000428061.2:c.200A>G ENSP00000412441.2:p.Asn67Ser
ENST00000474897.5:c.200A>G ENSP00000434235.1:p.Asn67Ser
ENST00000610387.4:c.200A>G ENSP00000482091.1:p.Asn67Ser
NM_001127649.2:c.200A>G NP_001121121.1:p.Asn67Ser
NM_001199319.1:c.200A>G NP_001186248.1:p.Asn67Ser
NM_017929.5:c.200A>G NP_060399.1:p.Asn67Ser
NM_001127649.3:c.200A>G MANE Select NP_001121121.1:p.Asn67Ser
NM_001199319.2:c.200A>G NP_001186248.1:p.Asn67Ser
NM_017929.6:c.200A>G NP_060399.1:p.Asn67Ser