Canonical Allele Identifier: CA368203074
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92519032T>A , CM000669.2:g.92519032T>A GRCh38
NC_000007.13:g.92148346T>A , CM000669.1:g.92148346T>A GRCh37
NC_000007.12:g.91986282T>A NCBI36
NG_008341.1:g.14500A>T
NG_008341.2:g.14500A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.320A>T MANE Select ENSP00000248633.4:p.Glu107Val
ENST00000248633.8:c.320A>T ENSP00000248633.4:p.Glu107Val
ENST00000428214.5:c.320A>T ENSP00000394413.1:p.Glu107Val
ENST00000438045.5:c.273+3070A>T ENSP00000410438.1:n.273+3070A>T
ENST00000484913.5:n.324A>T
NM_000466.2:c.320A>T NP_000457.1:p.Glu107Val
NM_001282677.1:c.320A>T NP_001269606.1:p.Glu107Val
NM_001282678.1:c.-340A>T NP_001269607.1:n.-340A>T
XR_242246.3:n.416A>T
XR_242246.5:n.367A>T
NM_000466.3:c.320A>T MANE Select NP_000457.1:p.Glu107Val
NM_001282677.2:c.320A>T NP_001269606.1:p.Glu107Val
NM_001282678.2:c.-340A>T NP_001269607.1:n.-340A>T