Canonical Allele Identifier: CA161951571

Linked Data

dbSNP Id: rs182526018
gnomAD v3: 7-92489160-G-A
gnomAD v4: 7-92489160-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489160G>A , CM000669.2:g.92489160G>A GRCh38
NC_000007.13:g.92118474G>A , CM000669.1:g.92118474G>A GRCh37
NC_000007.12:g.91956410G>A NCBI36
NG_008341.1:g.44372C>T
NG_008341.2:g.44372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3767+133C>T (PEX1) MANE Select ENSP00000248633.4:n.3767+133C>T
ENST00000248633.8:c.3767+133C>T (PEX1) ENSP00000248633.4:n.3767+133C>T
ENST00000428214.5:c.3596+133C>T (PEX1) ENSP00000394413.1:n.3596+133C>T
ENST00000438045.5:c.2801+133C>T (PEX1) ENSP00000410438.1:n.2801+133C>T
ENST00000477342.1:n.502+133C>T (PEX1)
ENST00000484913.5:n.3806+133C>T (PEX1)
ENST00000496420.5:n.4817+133C>T (PEX1)
NM_000466.2:c.3767+133C>T (PEX1) NP_000457.1:n.3767+133C>T
NM_001282677.1:c.3596+133C>T (PEX1) NP_001269606.1:n.3596+133C>T
NM_001282678.1:c.3143+133C>T (PEX1) NP_001269607.1:n.3143+133C>T
XM_005250433.3:c.2018+133C>T (PEX1) XP_005250490.1:n.2018+133C>T
XR_242246.3:n.3858+133C>T (PEX1)
XR_927494.1:n.1036-2083G>A (GATAD1)
XR_927495.1:n.1036-926G>A (GATAD1)
XR_927496.1:n.1041-2083G>A (GATAD1)
XR_927497.1:n.1036-926G>A (GATAD1)
XR_927498.1:n.1124-2083G>A (GATAD1)
XR_927500.1:n.1033-2083G>A (GATAD1)
XR_927502.1:n.1033-926G>A (GATAD1)
XR_927503.1:n.967-2083G>A (GATAD1)
XM_017012319.2:c.2018+133C>T (PEX1) XP_016867808.1:n.2018+133C>T
XR_001744808.2:n.2789+133C>T (PEX1)
XR_001744842.2:n.2281-2083G>A (GATAD1)
XR_001744843.2:n.2212-2083G>A (GATAD1)
XR_002956472.1:n.2281-926G>A (GATAD1)
XR_002956473.1:n.2369-2083G>A (GATAD1)
XR_002956474.1:n.2286-2083G>A (GATAD1)
XR_242246.5:n.3809+133C>T (PEX1)
XR_927494.3:n.1063-2083G>A (GATAD1)
XR_927500.3:n.1060-2083G>A (GATAD1)
XR_927503.3:n.994-2083G>A (GATAD1)
NM_000466.3:c.3767+133C>T (PEX1) MANE Select NP_000457.1:n.3767+133C>T
NM_001282677.2:c.3596+133C>T (PEX1) NP_001269606.1:n.3596+133C>T
NM_001282678.2:c.3143+133C>T (PEX1) NP_001269607.1:n.3143+133C>T