Canonical Allele Identifier: CA368164751

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491469G>T , CM000669.2:g.92491469G>T GRCh38
NC_000007.13:g.92120783G>T , CM000669.1:g.92120783G>T GRCh37
NC_000007.12:g.91958719G>T NCBI36
NG_008341.1:g.42063C>A
NG_008341.2:g.42063C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3241C>A (PEX1) MANE Select ENSP00000248633.4:p.Leu1081Met
ENST00000248633.8:c.3241C>A (PEX1) ENSP00000248633.4:p.Leu1081Met
ENST00000428214.5:c.3070C>A (PEX1) ENSP00000394413.1:p.Leu1024Met
ENST00000438045.5:c.2275C>A (PEX1) ENSP00000410438.1:p.Leu759Met
ENST00000484913.5:n.3280C>A (PEX1)
ENST00000496420.5:n.4296C>A (PEX1)
NM_000466.2:c.3241C>A (PEX1) NP_000457.1:p.Leu1081Met
NM_001282677.1:c.3070C>A (PEX1) NP_001269606.1:p.Leu1024Met
NM_001282678.1:c.2617C>A (PEX1) NP_001269607.1:p.Leu873Met
XM_005250433.3:c.1492C>A (PEX1) XP_005250490.1:p.Leu498Met
XR_242246.3:n.3337C>A (PEX1)
XM_017012319.2:c.1492C>A (PEX1) XP_016867808.1:p.Leu498Met
XR_001744808.2:n.2268C>A (PEX1)
XR_001744842.2:n.2507G>T (GATAD1)
XR_001744843.2:n.2438G>T (GATAD1)
XR_002956472.1:n.2564G>T (GATAD1)
XR_002956473.1:n.2595G>T (GATAD1)
XR_002956474.1:n.2512G>T (GATAD1)
XR_242246.5:n.3288C>A (PEX1)
XR_927494.3:n.1289G>T (GATAD1)
XR_927500.3:n.1286G>T (GATAD1)
XR_927503.3:n.1220G>T (GATAD1)
NM_000466.3:c.3241C>A (PEX1) MANE Select NP_000457.1:p.Leu1081Met
NM_001282677.2:c.3070C>A (PEX1) NP_001269606.1:p.Leu1024Met
NM_001282678.2:c.2617C>A (PEX1) NP_001269607.1:p.Leu873Met