Canonical Allele Identifier: CA1725935154
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499711C= , CM000669.2:g.92499711C= GRCh38
NC_000007.13:g.92129025C= , CM000669.1:g.92129025C= GRCh37
NC_000007.12:g.91966961C= NCBI36
NG_008341.1:g.33821G=
NG_008341.2:g.33821G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2711G= MANE Select ENSP00000248633.4:p.Ser904=
ENST00000248633.8:c.2711G= ENSP00000248633.4:p.Ser904=
ENST00000428214.5:c.2540G= ENSP00000394413.1:p.Ser847=
ENST00000438045.5:c.1745G= ENSP00000410438.1:p.Ser582=
ENST00000484913.5:n.2750G=
ENST00000496420.5:n.2603G=
NM_000466.2:c.2711G= NP_000457.1:p.Ser904=
NM_001282677.1:c.2540G= NP_001269606.1:p.Ser847=
NM_001282678.1:c.2087G= NP_001269607.1:p.Ser696=
XM_005250433.3:c.962G= XP_005250490.1:p.Ser321=
XR_242246.3:n.2807G=
XM_017012319.2:c.962G= XP_016867808.1:p.Ser321=
XR_001744808.2:n.1738G=
XR_242246.5:n.2758G=
NM_000466.3:c.2711G= MANE Select NP_000457.1:p.Ser904=
NM_001282677.2:c.2540G= NP_001269606.1:p.Ser847=
NM_001282678.2:c.2087G= NP_001269607.1:p.Ser696=