Canonical Allele Identifier: CA1725941016
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92506222T= , CM000669.2:g.92506222T= GRCh38
NC_000007.13:g.92135536T= , CM000669.1:g.92135536T= GRCh37
NC_000007.12:g.91973472T= NCBI36
NG_008341.1:g.27310A=
NG_008341.2:g.27310A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1900+26A= MANE Select ENSP00000248633.4:n.1900+26A=
ENST00000248633.8:c.1900+26A= ENSP00000248633.4:n.1900+26A=
ENST00000422866.1:c.718+26A=
ENST00000428214.5:c.1900+26A= ENSP00000394413.1:n.1900+26A=
ENST00000438045.5:c.934+26A= ENSP00000410438.1:n.934+26A=
ENST00000484913.5:n.1939+26A=
ENST00000496420.5:n.1576+26A=
NM_000466.2:c.1900+26A= NP_000457.1:n.1900+26A=
NM_001282677.1:c.1900+26A= NP_001269606.1:n.1900+26A=
NM_001282678.1:c.1276+26A= NP_001269607.1:n.1276+26A=
XM_005250433.3:c.151+26A= XP_005250490.1:n.151+26A=
XR_242246.3:n.1996+26A=
XM_017012319.2:c.151+26A= XP_016867808.1:n.151+26A=
XR_001744808.2:n.927+26A=
XR_242246.5:n.1947+26A=
NM_000466.3:c.1900+26A= MANE Select NP_000457.1:n.1900+26A=
NM_001282677.2:c.1900+26A= NP_001269606.1:n.1900+26A=
NM_001282678.2:c.1276+26A= NP_001269607.1:n.1276+26A=