Canonical Allele Identifier: CA1624312405
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969554G= , CM000668.2:g.42969554G= GRCh38
NC_000006.11:g.42937292G= , CM000668.1:g.42937292G= GRCh37
NC_000006.10:g.43045270G= NCBI36
NG_008370.1:g.14690C=

Transcript Alleles

HGVS Amino-acid change
ENST00000304611.13:c.1367+114C= MANE Select ENSP00000303511.8:n.1367+114C=
ENST00000244546.4:c.1367+114C= ENSP00000244546.4:n.1367+114C=
ENST00000304611.12:c.1367+114C= ENSP00000303511.8:n.1367+114C=
NM_000287.3:c.1367+114C= NP_000278.3:n.1367+114C=
NM_001316313.1:c.1103+114C= NP_001303242.1:n.1103+114C=
NR_133009.1:n.1460+114C=
XM_011514661.1:c.1283+114C= XP_011512963.1:n.1283+114C=
XR_926246.1:n.1460+114C=
XM_011514661.2:c.1283+114C= XP_011512963.1:n.1283+114C=
XR_001743466.2:n.2441+114C=
NM_000287.4:c.1367+114C= MANE Select NP_000278.3:n.1367+114C=
NM_001316313.2:c.1103+114C= NP_001303242.1:n.1103+114C=
NR_133009.2:n.1398+114C=