Canonical Allele Identifier: CA368160966

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489741G>C , CM000669.2:g.92489741G>C GRCh38
NC_000007.13:g.92119055G>C , CM000669.1:g.92119055G>C GRCh37
NC_000007.12:g.91956991G>C NCBI36
NG_008341.1:g.43791C>G
NG_008341.2:g.43791C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3609C>G (PEX1) MANE Select ENSP00000248633.4:p.Ile1203Met
ENST00000248633.8:c.3609C>G (PEX1) ENSP00000248633.4:p.Ile1203Met
ENST00000428214.5:c.3438C>G (PEX1) ENSP00000394413.1:p.Ile1146Met
ENST00000438045.5:c.2643C>G (PEX1) ENSP00000410438.1:p.Ile881Met
ENST00000469417.1:n.506C>G (PEX1)
ENST00000477342.1:n.54C>G (PEX1)
ENST00000484913.5:n.3648C>G (PEX1)
ENST00000496420.5:n.4664C>G (PEX1)
NM_000466.2:c.3609C>G (PEX1) NP_000457.1:p.Ile1203Met
NM_001282677.1:c.3438C>G (PEX1) NP_001269606.1:p.Ile1146Met
NM_001282678.1:c.2985C>G (PEX1) NP_001269607.1:p.Ile995Met
XM_005250433.3:c.1860C>G (PEX1) XP_005250490.1:p.Ile620Met
XR_242246.3:n.3705C>G (PEX1)
XR_927494.1:n.1036-1502G>C (GATAD1)
XR_927495.1:n.1036-345G>C (GATAD1)
XR_927496.1:n.1041-1502G>C (GATAD1)
XR_927497.1:n.1036-345G>C (GATAD1)
XR_927498.1:n.1124-1502G>C (GATAD1)
XR_927500.1:n.1033-1502G>C (GATAD1)
XR_927502.1:n.1033-345G>C (GATAD1)
XR_927503.1:n.967-1502G>C (GATAD1)
XM_017012319.2:c.1860C>G (PEX1) XP_016867808.1:p.Ile620Met
XR_001744808.2:n.2636C>G (PEX1)
XR_001744842.2:n.2281-1502G>C (GATAD1)
XR_001744843.2:n.2212-1502G>C (GATAD1)
XR_002956472.1:n.2281-345G>C (GATAD1)
XR_002956473.1:n.2369-1502G>C (GATAD1)
XR_002956474.1:n.2286-1502G>C (GATAD1)
XR_242246.5:n.3656C>G (PEX1)
XR_927494.3:n.1063-1502G>C (GATAD1)
XR_927500.3:n.1060-1502G>C (GATAD1)
XR_927503.3:n.994-1502G>C (GATAD1)
NM_000466.3:c.3609C>G (PEX1) MANE Select NP_000457.1:p.Ile1203Met
NM_001282677.2:c.3438C>G (PEX1) NP_001269606.1:p.Ile1146Met
NM_001282678.2:c.2985C>G (PEX1) NP_001269607.1:p.Ile995Met