Canonical Allele Identifier: CA1725931036

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494306G= , CM000669.2:g.92494306G= GRCh38
NC_000007.13:g.92123620G= , CM000669.1:g.92123620G= GRCh37
NC_000007.12:g.91961556G= NCBI36
NG_008341.1:g.39226C=
NG_008341.2:g.39226C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3017C= (PEX1) MANE Select ENSP00000248633.4:p.Pro1006=
ENST00000248633.8:c.3017C= (PEX1) ENSP00000248633.4:p.Pro1006=
ENST00000428214.5:c.2846C= (PEX1) ENSP00000394413.1:p.Pro949=
ENST00000438045.5:c.2051C= (PEX1) ENSP00000410438.1:p.Pro684=
ENST00000484913.5:n.3056C= (PEX1)
ENST00000496420.5:n.2909C= (PEX1)
NM_000466.2:c.3017C= (PEX1) NP_000457.1:p.Pro1006=
NM_001282677.1:c.2846C= (PEX1) NP_001269606.1:p.Pro949=
NM_001282678.1:c.2393C= (PEX1) NP_001269607.1:p.Pro798=
XM_005250433.3:c.1268C= (PEX1) XP_005250490.1:p.Pro423=
XR_242246.3:n.3113C= (PEX1)
XM_017012319.2:c.1268C= (PEX1) XP_016867808.1:p.Pro423=
XR_001744808.2:n.2044C= (PEX1)
XR_001744843.2:n.5275G= (GATAD1)
XR_242246.5:n.3064C= (PEX1)
XR_927494.3:n.4126G= (GATAD1)
XR_927503.3:n.4057G= (GATAD1)
NM_000466.3:c.3017C= (PEX1) MANE Select NP_000457.1:p.Pro1006=
NM_001282677.2:c.2846C= (PEX1) NP_001269606.1:p.Pro949=
NM_001282678.2:c.2393C= (PEX1) NP_001269607.1:p.Pro798=