Canonical Allele Identifier: CA1624312639
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969721C= , CM000668.2:g.42969721C= GRCh38
NC_000006.11:g.42937459C= , CM000668.1:g.42937459C= GRCh37
NC_000006.10:g.43045437C= NCBI36
NG_008370.1:g.14523G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1314G= MANE Select ENSP00000303511.8:p.Leu438=
ENST00000244546.4:c.1314G= ENSP00000244546.4:p.Leu438=
ENST00000304611.12:c.1314G= ENSP00000303511.8:p.Leu438=
NM_000287.3:c.1314G= NP_000278.3:p.Leu438=
NM_001316313.1:c.1050G= NP_001303242.1:p.Leu350=
NR_133009.1:n.1407G=
XM_011514661.1:c.1230G= XP_011512963.1:p.Leu410=
XR_926246.1:n.1407G=
XM_011514661.2:c.1230G= XP_011512963.1:p.Leu410=
XR_001743466.2:n.2388G=
NM_000287.4:c.1314G= MANE Select NP_000278.3:p.Leu438=
NM_001316313.2:c.1050G= NP_001303242.1:p.Leu350=
NR_133009.2:n.1345G=