Canonical Allele Identifier: CA1725935153
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499710A= , CM000669.2:g.92499710A= GRCh38
NC_000007.13:g.92129024A= , CM000669.1:g.92129024A= GRCh37
NC_000007.12:g.91966960A= NCBI36
NG_008341.1:g.33822T=
NG_008341.2:g.33822T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2712T= MANE Select ENSP00000248633.4:p.Ser904=
ENST00000248633.8:c.2712T= ENSP00000248633.4:p.Ser904=
ENST00000428214.5:c.2541T= ENSP00000394413.1:p.Ser847=
ENST00000438045.5:c.1746T= ENSP00000410438.1:p.Ser582=
ENST00000484913.5:n.2751T=
ENST00000496420.5:n.2604T=
NM_000466.2:c.2712T= NP_000457.1:p.Ser904=
NM_001282677.1:c.2541T= NP_001269606.1:p.Ser847=
NM_001282678.1:c.2088T= NP_001269607.1:p.Ser696=
XM_005250433.3:c.963T= XP_005250490.1:p.Ser321=
XR_242246.3:n.2808T=
XM_017012319.2:c.963T= XP_016867808.1:p.Ser321=
XR_001744808.2:n.1739T=
XR_242246.5:n.2759T=
NM_000466.3:c.2712T= MANE Select NP_000457.1:p.Ser904=
NM_001282677.2:c.2541T= NP_001269606.1:p.Ser847=
NM_001282678.2:c.2088T= NP_001269607.1:p.Ser696=