Canonical Allele Identifier: CA410264936
Gene: PEX26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078528T>C , CM000684.2:g.18078528T>C GRCh38
NC_000022.10:g.18561294T>C , CM000684.1:g.18561294T>C GRCh37
NC_000022.9:g.16941294T>C NCBI36
NG_008339.1:g.5609T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.152T>C MANE Select ENSP00000382648.4:p.Phe51Ser
ENST00000474897.6:c.152T>C ENSP00000434235.2:p.Phe51Ser
ENST00000329627.11:c.152T>C ENSP00000331106.5:p.Phe51Ser
ENST00000399744.7:c.152T>C ENSP00000382648.3:p.Phe51Ser
ENST00000428061.2:c.152T>C ENSP00000412441.2:p.Phe51Ser
ENST00000474897.5:c.152T>C ENSP00000434235.1:p.Phe51Ser
ENST00000610387.4:c.152T>C ENSP00000482091.1:p.Phe51Ser
NM_001127649.2:c.152T>C NP_001121121.1:p.Phe51Ser
NM_001199319.1:c.152T>C NP_001186248.1:p.Phe51Ser
NM_017929.5:c.152T>C NP_060399.1:p.Phe51Ser
NM_001127649.3:c.152T>C MANE Select NP_001121121.1:p.Phe51Ser
NM_001199319.2:c.152T>C NP_001186248.1:p.Phe51Ser
NM_017929.6:c.152T>C NP_060399.1:p.Phe51Ser