Canonical Allele Identifier: CA1624312650
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969722A= , CM000668.2:g.42969722A= GRCh38
NC_000006.11:g.42937460A= , CM000668.1:g.42937460A= GRCh37
NC_000006.10:g.43045438A= NCBI36
NG_008370.1:g.14522T=

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1313T= MANE Select ENSP00000303511.8:p.Leu438=
ENST00000244546.4:c.1313T= ENSP00000244546.4:p.Leu438=
ENST00000304611.12:c.1313T= ENSP00000303511.8:p.Leu438=
NM_000287.3:c.1313T= NP_000278.3:p.Leu438=
NM_001316313.1:c.1049T= NP_001303242.1:p.Leu350=
NR_133009.1:n.1406T=
XM_011514661.1:c.1229T= XP_011512963.1:p.Leu410=
XR_926246.1:n.1406T=
XM_011514661.2:c.1229T= XP_011512963.1:p.Leu410=
XR_001743466.2:n.2387T=
NM_000287.4:c.1313T= MANE Select NP_000278.3:p.Leu438=
NM_001316313.2:c.1049T= NP_001303242.1:p.Leu350=
NR_133009.2:n.1344T=