Canonical Allele Identifier: CA576302680

Linked Data

dbSNP Id: rs1423312452
gnomAD v2: 7-92118355-A-C
gnomAD v3: 7-92489041-A-C
gnomAD v4: 7-92489041-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489041A>C , CM000669.2:g.92489041A>C GRCh38
NC_000007.13:g.92118355A>C , CM000669.1:g.92118355A>C GRCh37
NC_000007.12:g.91956291A>C NCBI36
NG_008341.1:g.44491T>G
NG_008341.2:g.44491T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3767+252T>G (PEX1) MANE Select ENSP00000248633.4:n.3767+252T>G
ENST00000248633.8:c.3767+252T>G (PEX1) ENSP00000248633.4:n.3767+252T>G
ENST00000428214.5:c.3596+252T>G (PEX1) ENSP00000394413.1:n.3596+252T>G
ENST00000438045.5:c.2801+252T>G (PEX1) ENSP00000410438.1:n.2801+252T>G
ENST00000477342.1:n.502+252T>G (PEX1)
ENST00000484913.5:n.3806+252T>G (PEX1)
ENST00000496420.5:n.4817+252T>G (PEX1)
NM_000466.2:c.3767+252T>G (PEX1) NP_000457.1:n.3767+252T>G
NM_001282677.1:c.3596+252T>G (PEX1) NP_001269606.1:n.3596+252T>G
NM_001282678.1:c.3143+252T>G (PEX1) NP_001269607.1:n.3143+252T>G
XM_005250433.3:c.2018+252T>G (PEX1) XP_005250490.1:n.2018+252T>G
XR_242246.3:n.3858+252T>G (PEX1)
XR_927494.1:n.1036-2202A>C (GATAD1)
XR_927495.1:n.1036-1045A>C (GATAD1)
XR_927496.1:n.1041-2202A>C (GATAD1)
XR_927497.1:n.1036-1045A>C (GATAD1)
XR_927498.1:n.1124-2202A>C (GATAD1)
XR_927500.1:n.1033-2202A>C (GATAD1)
XR_927502.1:n.1033-1045A>C (GATAD1)
XR_927503.1:n.967-2202A>C (GATAD1)
XM_017012319.2:c.2018+252T>G (PEX1) XP_016867808.1:n.2018+252T>G
XR_001744808.2:n.2789+252T>G (PEX1)
XR_001744842.2:n.2281-2202A>C (GATAD1)
XR_001744843.2:n.2212-2202A>C (GATAD1)
XR_002956472.1:n.2281-1045A>C (GATAD1)
XR_002956473.1:n.2369-2202A>C (GATAD1)
XR_002956474.1:n.2286-2202A>C (GATAD1)
XR_242246.5:n.3809+252T>G (PEX1)
XR_927494.3:n.1063-2202A>C (GATAD1)
XR_927500.3:n.1060-2202A>C (GATAD1)
XR_927503.3:n.994-2202A>C (GATAD1)
NM_000466.3:c.3767+252T>G (PEX1) MANE Select NP_000457.1:n.3767+252T>G
NM_001282677.2:c.3596+252T>G (PEX1) NP_001269606.1:n.3596+252T>G
NM_001282678.2:c.3143+252T>G (PEX1) NP_001269607.1:n.3143+252T>G