Canonical Allele Identifier: CA1624312655
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969724G= , CM000668.2:g.42969724G= GRCh38
NC_000006.11:g.42937462G= , CM000668.1:g.42937462G= GRCh37
NC_000006.10:g.43045440G= NCBI36
NG_008370.1:g.14520C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1311C= MANE Select ENSP00000303511.8:p.Gly437=
ENST00000244546.4:c.1311C= ENSP00000244546.4:p.Gly437=
ENST00000304611.12:c.1311C= ENSP00000303511.8:p.Gly437=
NM_000287.3:c.1311C= NP_000278.3:p.Gly437=
NM_001316313.1:c.1047C= NP_001303242.1:p.Gly349=
NR_133009.1:n.1404C=
XM_011514661.1:c.1227C= XP_011512963.1:p.Gly409=
XR_926246.1:n.1404C=
XM_011514661.2:c.1227C= XP_011512963.1:p.Gly409=
XR_001743466.2:n.2385C=
NM_000287.4:c.1311C= MANE Select NP_000278.3:p.Gly437=
NM_001316313.2:c.1047C= NP_001303242.1:p.Gly349=
NR_133009.2:n.1342C=