Canonical Allele Identifier: CA1725947143
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517282T= , CM000669.2:g.92517282T= GRCh38
NC_000007.13:g.92146596T= , CM000669.1:g.92146596T= GRCh37
NC_000007.12:g.91984532T= NCBI36
NG_008341.1:g.16250A=
NG_008341.2:g.16250A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1233A= MANE Select ENSP00000248633.4:p.Lys411=
ENST00000248633.8:c.1233A= ENSP00000248633.4:p.Lys411=
ENST00000422866.1:c.134A=
ENST00000428214.5:c.1233A= ENSP00000394413.1:p.Lys411=
ENST00000438045.5:c.274-3315A= ENSP00000410438.1:n.274-3315A=
ENST00000484913.5:n.1272A=
NM_000466.2:c.1233A= NP_000457.1:p.Lys411=
NM_001282677.1:c.1233A= NP_001269606.1:p.Lys411=
NM_001282678.1:c.609A= NP_001269607.1:p.Lys203=
XR_242246.3:n.1329A=
XM_017012319.2:c.-434A= XP_016867808.1:n.-434A=
XR_001744808.2:n.343A=
XR_242246.5:n.1280A=
NM_000466.3:c.1233A= MANE Select NP_000457.1:p.Lys411=
NM_001282677.2:c.1233A= NP_001269606.1:p.Lys411=
NM_001282678.2:c.609A= NP_001269607.1:p.Lys203=