Canonical Allele Identifier: CA1725936119
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92501997T= , CM000669.2:g.92501997T= GRCh38
NC_000007.13:g.92131311T= , CM000669.1:g.92131311T= GRCh37
NC_000007.12:g.91969247T= NCBI36
NG_008341.1:g.31535A=
NG_008341.2:g.31535A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2309A= MANE Select ENSP00000248633.4:p.Gln770=
ENST00000248633.8:c.2309A= ENSP00000248633.4:p.Gln770=
ENST00000428214.5:c.2138A= ENSP00000394413.1:p.Gln713=
ENST00000438045.5:c.1343A= ENSP00000410438.1:p.Gln448=
ENST00000484913.5:n.2348A=
ENST00000496092.1:n.107A=
ENST00000496420.5:n.1985A=
NM_000466.2:c.2309A= NP_000457.1:p.Gln770=
NM_001282677.1:c.2138A= NP_001269606.1:p.Gln713=
NM_001282678.1:c.1685A= NP_001269607.1:p.Gln562=
XM_005250433.3:c.560A= XP_005250490.1:p.Gln187=
XR_242246.3:n.2405A=
XM_017012319.2:c.560A= XP_016867808.1:p.Gln187=
XR_001744808.2:n.1336A=
XR_242246.5:n.2356A=
NM_000466.3:c.2309A= MANE Select NP_000457.1:p.Gln770=
NM_001282677.2:c.2138A= NP_001269606.1:p.Gln713=
NM_001282678.2:c.1685A= NP_001269607.1:p.Gln562=