Canonical Allele Identifier: CA1624312482
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969638C= , CM000668.2:g.42969638C= GRCh38
NC_000006.11:g.42937376C= , CM000668.1:g.42937376C= GRCh37
NC_000006.10:g.43045354C= NCBI36
NG_008370.1:g.14606G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1367+30G= MANE Select ENSP00000303511.8:n.1367+30G=
ENST00000244546.4:c.1367+30G= ENSP00000244546.4:n.1367+30G=
ENST00000304611.12:c.1367+30G= ENSP00000303511.8:n.1367+30G=
NM_000287.3:c.1367+30G= NP_000278.3:n.1367+30G=
NM_001316313.1:c.1103+30G= NP_001303242.1:n.1103+30G=
NR_133009.1:n.1460+30G=
XM_011514661.1:c.1283+30G= XP_011512963.1:n.1283+30G=
XR_926246.1:n.1460+30G=
XM_011514661.2:c.1283+30G= XP_011512963.1:n.1283+30G=
XR_001743466.2:n.2441+30G=
NM_000287.4:c.1367+30G= MANE Select NP_000278.3:n.1367+30G=
NM_001316313.2:c.1103+30G= NP_001303242.1:n.1103+30G=
NR_133009.2:n.1398+30G=