Canonical Allele Identifier: CA1725931032

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494304G= , CM000669.2:g.92494304G= GRCh38
NC_000007.13:g.92123618G= , CM000669.1:g.92123618G= GRCh37
NC_000007.12:g.91961554G= NCBI36
NG_008341.1:g.39228C=
NG_008341.2:g.39228C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3019C= (PEX1) MANE Select ENSP00000248633.4:p.Pro1007=
ENST00000248633.8:c.3019C= (PEX1) ENSP00000248633.4:p.Pro1007=
ENST00000428214.5:c.2848C= (PEX1) ENSP00000394413.1:p.Pro950=
ENST00000438045.5:c.2053C= (PEX1) ENSP00000410438.1:p.Pro685=
ENST00000484913.5:n.3058C= (PEX1)
ENST00000496420.5:n.2911C= (PEX1)
NM_000466.2:c.3019C= (PEX1) NP_000457.1:p.Pro1007=
NM_001282677.1:c.2848C= (PEX1) NP_001269606.1:p.Pro950=
NM_001282678.1:c.2395C= (PEX1) NP_001269607.1:p.Pro799=
XM_005250433.3:c.1270C= (PEX1) XP_005250490.1:p.Pro424=
XR_242246.3:n.3115C= (PEX1)
XM_017012319.2:c.1270C= (PEX1) XP_016867808.1:p.Pro424=
XR_001744808.2:n.2046C= (PEX1)
XR_001744843.2:n.5273G= (GATAD1)
XR_242246.5:n.3066C= (PEX1)
XR_927494.3:n.4124G= (GATAD1)
XR_927503.3:n.4055G= (GATAD1)
NM_000466.3:c.3019C= (PEX1) MANE Select NP_000457.1:p.Pro1007=
NM_001282677.2:c.2848C= (PEX1) NP_001269606.1:p.Pro950=
NM_001282678.2:c.2395C= (PEX1) NP_001269607.1:p.Pro799=