Canonical Allele Identifier: CA1725947802
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517728T= , CM000669.2:g.92517728T= GRCh38
NC_000007.13:g.92147042T= , CM000669.1:g.92147042T= GRCh37
NC_000007.12:g.91984978T= NCBI36
NG_008341.1:g.15804A=
NG_008341.2:g.15804A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.787A= MANE Select ENSP00000248633.4:p.Thr263=
ENST00000248633.8:c.787A= ENSP00000248633.4:p.Thr263=
ENST00000428214.5:c.787A= ENSP00000394413.1:p.Thr263=
ENST00000438045.5:c.274-3761A= ENSP00000410438.1:n.274-3761A=
ENST00000484913.5:n.826A=
NM_000466.2:c.787A= NP_000457.1:p.Thr263=
NM_001282677.1:c.787A= NP_001269606.1:p.Thr263=
NM_001282678.1:c.163A= NP_001269607.1:p.Thr55=
XR_242246.3:n.883A=
XR_242246.5:n.834A=
NM_000466.3:c.787A= MANE Select NP_000457.1:p.Thr263=
NM_001282677.2:c.787A= NP_001269606.1:p.Thr263=
NM_001282678.2:c.163A= NP_001269607.1:p.Thr55=