Canonical Allele Identifier: CA368168526

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494544T>C , CM000669.2:g.92494544T>C GRCh38
NC_000007.13:g.92123858T>C , CM000669.1:g.92123858T>C GRCh37
NC_000007.12:g.91961794T>C NCBI36
NG_008341.1:g.38988A>G
NG_008341.2:g.38988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2869A>G (PEX1) MANE Select ENSP00000248633.4:p.Thr957Ala
ENST00000248633.8:c.2869A>G (PEX1) ENSP00000248633.4:p.Thr957Ala
ENST00000428214.5:c.2698A>G (PEX1) ENSP00000394413.1:p.Thr900Ala
ENST00000438045.5:c.1903A>G (PEX1) ENSP00000410438.1:p.Thr635Ala
ENST00000484913.5:n.2908A>G (PEX1)
ENST00000496420.5:n.2761A>G (PEX1)
NM_000466.2:c.2869A>G (PEX1) NP_000457.1:p.Thr957Ala
NM_001282677.1:c.2698A>G (PEX1) NP_001269606.1:p.Thr900Ala
NM_001282678.1:c.2245A>G (PEX1) NP_001269607.1:p.Thr749Ala
XM_005250433.3:c.1120A>G (PEX1) XP_005250490.1:p.Thr374Ala
XR_242246.3:n.2965A>G (PEX1)
XM_017012319.2:c.1120A>G (PEX1) XP_016867808.1:p.Thr374Ala
XR_001744808.2:n.1896A>G (PEX1)
XR_001744843.2:n.5513T>C (GATAD1)
XR_242246.5:n.2916A>G (PEX1)
XR_927494.3:n.4364T>C (GATAD1)
XR_927503.3:n.4295T>C (GATAD1)
NM_000466.3:c.2869A>G (PEX1) MANE Select NP_000457.1:p.Thr957Ala
NM_001282677.2:c.2698A>G (PEX1) NP_001269606.1:p.Thr900Ala
NM_001282678.2:c.2245A>G (PEX1) NP_001269607.1:p.Thr749Ala