Canonical Allele Identifier: CA364155907
Gene: PEX6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969784G>T , CM000668.2:g.42969784G>T GRCh38
NC_000006.11:g.42937522G>T , CM000668.1:g.42937522G>T GRCh37
NC_000006.10:g.43045500G>T NCBI36
NG_008370.1:g.14460C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1251C>A MANE Select ENSP00000303511.8:p.Ser417Arg
ENST00000244546.4:c.1251C>A ENSP00000244546.4:p.Ser417Arg
ENST00000304611.12:c.1251C>A ENSP00000303511.8:p.Ser417Arg
NM_000287.3:c.1251C>A NP_000278.3:p.Ser417Arg
NM_001316313.1:c.987C>A NP_001303242.1:p.Ser329Arg
NR_133009.1:n.1344C>A
XM_011514661.1:c.1167C>A XP_011512963.1:p.Ser389Arg
XR_926246.1:n.1344C>A
XM_011514661.2:c.1167C>A XP_011512963.1:p.Ser389Arg
XR_001743466.2:n.2325C>A
NM_000287.4:c.1251C>A MANE Select NP_000278.3:p.Ser417Arg
NM_001316313.2:c.987C>A NP_001303242.1:p.Ser329Arg
NR_133009.2:n.1282C>A