Canonical Allele Identifier: CA1725947904
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517795T= , CM000669.2:g.92517795T= GRCh38
NC_000007.13:g.92147109T= , CM000669.1:g.92147109T= GRCh37
NC_000007.12:g.91985045T= NCBI36
NG_008341.1:g.15737A=
NG_008341.2:g.15737A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.720A= MANE Select ENSP00000248633.4:p.Ser240=
ENST00000248633.8:c.720A= ENSP00000248633.4:p.Ser240=
ENST00000428214.5:c.720A= ENSP00000394413.1:p.Ser240=
ENST00000438045.5:c.274-3828A= ENSP00000410438.1:n.274-3828A=
ENST00000484913.5:n.759A=
NM_000466.2:c.720A= NP_000457.1:p.Ser240=
NM_001282677.1:c.720A= NP_001269606.1:p.Ser240=
NM_001282678.1:c.96A= NP_001269607.1:p.Ser32=
XR_242246.3:n.816A=
XR_242246.5:n.767A=
NM_000466.3:c.720A= MANE Select NP_000457.1:p.Ser240=
NM_001282677.2:c.720A= NP_001269606.1:p.Ser240=
NM_001282678.2:c.96A= NP_001269607.1:p.Ser32=