Canonical Allele Identifier: CA368164316

Linked Data

gnomAD v4: 7-92491427-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491427C>A , CM000669.2:g.92491427C>A GRCh38
NC_000007.13:g.92120741C>A , CM000669.1:g.92120741C>A GRCh37
NC_000007.12:g.91958677C>A NCBI36
NG_008341.1:g.42105G>T
NG_008341.2:g.42105G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3283G>T (PEX1) MANE Select ENSP00000248633.4:p.Asp1095Tyr
ENST00000248633.8:c.3283G>T (PEX1) ENSP00000248633.4:p.Asp1095Tyr
ENST00000428214.5:c.3112G>T (PEX1) ENSP00000394413.1:p.Asp1038Tyr
ENST00000438045.5:c.2317G>T (PEX1) ENSP00000410438.1:p.Asp773Tyr
ENST00000484913.5:n.3322G>T (PEX1)
ENST00000496420.5:n.4338G>T (PEX1)
NM_000466.2:c.3283G>T (PEX1) NP_000457.1:p.Asp1095Tyr
NM_001282677.1:c.3112G>T (PEX1) NP_001269606.1:p.Asp1038Tyr
NM_001282678.1:c.2659G>T (PEX1) NP_001269607.1:p.Asp887Tyr
XM_005250433.3:c.1534G>T (PEX1) XP_005250490.1:p.Asp512Tyr
XR_242246.3:n.3379G>T (PEX1)
XM_017012319.2:c.1534G>T (PEX1) XP_016867808.1:p.Asp512Tyr
XR_001744808.2:n.2310G>T (PEX1)
XR_001744842.2:n.2465C>A (GATAD1)
XR_001744843.2:n.2396C>A (GATAD1)
XR_002956472.1:n.2522C>A (GATAD1)
XR_002956473.1:n.2553C>A (GATAD1)
XR_002956474.1:n.2470C>A (GATAD1)
XR_242246.5:n.3330G>T (PEX1)
XR_927494.3:n.1247C>A (GATAD1)
XR_927500.3:n.1244C>A (GATAD1)
XR_927503.3:n.1178C>A (GATAD1)
NM_000466.3:c.3283G>T (PEX1) MANE Select NP_000457.1:p.Asp1095Tyr
NM_001282677.2:c.3112G>T (PEX1) NP_001269606.1:p.Asp1038Tyr
NM_001282678.2:c.2659G>T (PEX1) NP_001269607.1:p.Asp887Tyr