Canonical Allele Identifier: CA1725926767

Gene: PEX1 GATAD1

Linked Data

• dbSNP Id: rs1791157698
• gnomAD v4: 7-92489575-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92489575A>G , CM000669.2:g.92489575A>G	GRCh38
NC_000007.13:g.92118889A>G , CM000669.1:g.92118889A>G	GRCh37
NC_000007.12:g.91956825A>G	NCBI36
NG_008341.1:g.43957T>C
NG_008341.2:g.43957T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.3636+139T>C (PEX1) MANE Select	ENSP00000248633.4:n.3636+139T>C
ENST00000248633.8:c.3636+139T>C (PEX1)	ENSP00000248633.4:n.3636+139T>C
ENST00000428214.5:c.3465+139T>C (PEX1)	ENSP00000394413.1:n.3465+139T>C
ENST00000438045.5:c.2670+139T>C (PEX1)	ENSP00000410438.1:n.2670+139T>C
ENST00000469417.1:n.533+139T>C (PEX1)
ENST00000477342.1:n.220T>C (PEX1)
ENST00000484913.5:n.3675+139T>C (PEX1)
ENST00000496420.5:n.4686+144T>C (PEX1)
NM_000466.2:c.3636+139T>C (PEX1)	NP_000457.1:n.3636+139T>C
NM_001282677.1:c.3465+139T>C (PEX1)	NP_001269606.1:n.3465+139T>C
NM_001282678.1:c.3012+139T>C (PEX1)	NP_001269607.1:n.3012+139T>C
XM_005250433.3:c.1887+139T>C (PEX1)	XP_005250490.1:n.1887+139T>C
XR_242246.3:n.3727+144T>C (PEX1)
XR_927494.1:n.1036-1668A>G (GATAD1)
XR_927495.1:n.1036-511A>G (GATAD1)
XR_927496.1:n.1041-1668A>G (GATAD1)
XR_927497.1:n.1036-511A>G (GATAD1)
XR_927498.1:n.1124-1668A>G (GATAD1)
XR_927500.1:n.1033-1668A>G (GATAD1)
XR_927502.1:n.1033-511A>G (GATAD1)
XR_927503.1:n.967-1668A>G (GATAD1)
XM_017012319.2:c.1887+139T>C (PEX1)	XP_016867808.1:n.1887+139T>C
XR_001744808.2:n.2658+144T>C (PEX1)
XR_001744842.2:n.2281-1668A>G (GATAD1)
XR_001744843.2:n.2212-1668A>G (GATAD1)
XR_002956472.1:n.2281-511A>G (GATAD1)
XR_002956473.1:n.2369-1668A>G (GATAD1)
XR_002956474.1:n.2286-1668A>G (GATAD1)
XR_242246.5:n.3678+144T>C (PEX1)
XR_927494.3:n.1063-1668A>G (GATAD1)
XR_927500.3:n.1060-1668A>G (GATAD1)
XR_927503.3:n.994-1668A>G (GATAD1)
NM_000466.3:c.3636+139T>C (PEX1) MANE Select	NP_000457.1:n.3636+139T>C
NM_001282677.2:c.3465+139T>C (PEX1)	NP_001269606.1:n.3465+139T>C
NM_001282678.2:c.3012+139T>C (PEX1)	NP_001269607.1:n.3012+139T>C