Canonical Allele Identifier: CA1725947856
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517755A= , CM000669.2:g.92517755A= GRCh38
NC_000007.13:g.92147069A= , CM000669.1:g.92147069A= GRCh37
NC_000007.12:g.91985005A= NCBI36
NG_008341.1:g.15777T=
NG_008341.2:g.15777T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.760T= MANE Select ENSP00000248633.4:p.Ser254=
ENST00000248633.8:c.760T= ENSP00000248633.4:p.Ser254=
ENST00000428214.5:c.760T= ENSP00000394413.1:p.Ser254=
ENST00000438045.5:c.274-3788T= ENSP00000410438.1:n.274-3788T=
ENST00000484913.5:n.799T=
NM_000466.2:c.760T= NP_000457.1:p.Ser254=
NM_001282677.1:c.760T= NP_001269606.1:p.Ser254=
NM_001282678.1:c.136T= NP_001269607.1:p.Ser46=
XR_242246.3:n.856T=
XR_242246.5:n.807T=
NM_000466.3:c.760T= MANE Select NP_000457.1:p.Ser254=
NM_001282677.2:c.760T= NP_001269606.1:p.Ser254=
NM_001282678.2:c.136T= NP_001269607.1:p.Ser46=