Canonical Allele Identifier: CA364155831
Gene: PEX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969761T>A , CM000668.2:g.42969761T>A GRCh38
NC_000006.11:g.42937499T>A , CM000668.1:g.42937499T>A GRCh37
NC_000006.10:g.43045477T>A NCBI36
NG_008370.1:g.14483A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1274A>T MANE Select ENSP00000303511.8:p.Glu425Val
ENST00000244546.4:c.1274A>T ENSP00000244546.4:p.Glu425Val
ENST00000304611.12:c.1274A>T ENSP00000303511.8:p.Glu425Val
NM_000287.3:c.1274A>T NP_000278.3:p.Glu425Val
NM_001316313.1:c.1010A>T NP_001303242.1:p.Glu337Val
NR_133009.1:n.1367A>T
XM_011514661.1:c.1190A>T XP_011512963.1:p.Glu397Val
XR_926246.1:n.1367A>T
XM_011514661.2:c.1190A>T XP_011512963.1:p.Glu397Val
XR_001743466.2:n.2348A>T
NM_000287.4:c.1274A>T MANE Select NP_000278.3:p.Glu425Val
NM_001316313.2:c.1010A>T NP_001303242.1:p.Glu337Val
NR_133009.2:n.1305A>T