Canonical Allele Identifier: CA1624312420
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42969563A= , CM000668.2:g.42969563A= GRCh38
NC_000006.11:g.42937301A= , CM000668.1:g.42937301A= GRCh37
NC_000006.10:g.43045279A= NCBI36
NG_008370.1:g.14681T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304611.13:c.1367+105T= MANE Select ENSP00000303511.8:n.1367+105T=
ENST00000244546.4:c.1367+105T= ENSP00000244546.4:n.1367+105T=
ENST00000304611.12:c.1367+105T= ENSP00000303511.8:n.1367+105T=
NM_000287.3:c.1367+105T= NP_000278.3:n.1367+105T=
NM_001316313.1:c.1103+105T= NP_001303242.1:n.1103+105T=
NR_133009.1:n.1460+105T=
XM_011514661.1:c.1283+105T= XP_011512963.1:n.1283+105T=
XR_926246.1:n.1460+105T=
XM_011514661.2:c.1283+105T= XP_011512963.1:n.1283+105T=
XR_001743466.2:n.2441+105T=
NM_000287.4:c.1367+105T= MANE Select NP_000278.3:n.1367+105T=
NM_001316313.2:c.1103+105T= NP_001303242.1:n.1103+105T=
NR_133009.2:n.1398+105T=