Canonical Allele Identifier: CA1624310848
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42968239C= , CM000668.2:g.42968239C= GRCh38
NC_000006.11:g.42935977C= , CM000668.1:g.42935977C= GRCh37
NC_000006.10:g.43043955C= NCBI36
NG_008370.1:g.16005G=

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1688+51G= MANE Select ENSP00000303511.8:n.1688+51G=
ENST00000244546.4:c.1688+51G= ENSP00000244546.4:n.1688+51G=
ENST00000304611.12:c.1688+51G= ENSP00000303511.8:n.1688+51G=
NM_000287.3:c.1688+51G= NP_000278.3:n.1688+51G=
NM_001316313.1:c.1424+51G= NP_001303242.1:n.1424+51G=
NR_133009.1:n.1781+51G=
XM_011514661.1:c.1604+51G= XP_011512963.1:n.1604+51G=
XR_926246.1:n.1669+51G=
XM_011514661.2:c.1604+51G= XP_011512963.1:n.1604+51G=
XR_001743466.2:n.2650+51G=
NM_000287.4:c.1688+51G= MANE Select NP_000278.3:n.1688+51G=
NM_001316313.2:c.1424+51G= NP_001303242.1:n.1424+51G=
NR_133009.2:n.1719+51G=