Canonical Allele Identifier: CA456479508

Gene: PEX1 GATAD1

Linked Data

• ClinVar Variation Id: 1145140
• ClinVar RCV Id: RCV001483910
• dbSNP Id: rs2116039237
• gnomAD v4: 7-92489364-T-C
• MyVariant Identifiers: chr7:g.92118678T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92489364T>C , CM000669.2:g.92489364T>C	GRCh38
NC_000007.13:g.92118678T>C , CM000669.1:g.92118678T>C	GRCh37
NC_000007.12:g.91956614T>C	NCBI36
NG_008341.1:g.44168A>G
NG_008341.2:g.44168A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.3696A>G (PEX1) MANE Select	ENSP00000248633.4:p.Ser1232=
ENST00000248633.8:c.3696A>G (PEX1)	ENSP00000248633.4:p.Ser1232=
ENST00000428214.5:c.3525A>G (PEX1)	ENSP00000394413.1:p.Ser1175=
ENST00000438045.5:c.2730A>G (PEX1)	ENSP00000410438.1:p.Ser910=
ENST00000477342.1:n.431A>G (PEX1)
ENST00000484913.5:n.3735A>G (PEX1)
ENST00000496420.5:n.4746A>G (PEX1)
NM_000466.2:c.3696A>G (PEX1)	NP_000457.1:p.Ser1232=
NM_001282677.1:c.3525A>G (PEX1)	NP_001269606.1:p.Ser1175=
NM_001282678.1:c.3072A>G (PEX1)	NP_001269607.1:p.Ser1024=
XM_005250433.3:c.1947A>G (PEX1)	XP_005250490.1:p.Ser649=
XR_242246.3:n.3787A>G (PEX1)
XR_927494.1:n.1036-1879T>C (GATAD1)
XR_927495.1:n.1036-722T>C (GATAD1)
XR_927496.1:n.1041-1879T>C (GATAD1)
XR_927497.1:n.1036-722T>C (GATAD1)
XR_927498.1:n.1124-1879T>C (GATAD1)
XR_927500.1:n.1033-1879T>C (GATAD1)
XR_927502.1:n.1033-722T>C (GATAD1)
XR_927503.1:n.967-1879T>C (GATAD1)
XM_017012319.2:c.1947A>G (PEX1)	XP_016867808.1:p.Ser649=
XR_001744808.2:n.2718A>G (PEX1)
XR_001744842.2:n.2281-1879T>C (GATAD1)
XR_001744843.2:n.2212-1879T>C (GATAD1)
XR_002956472.1:n.2281-722T>C (GATAD1)
XR_002956473.1:n.2369-1879T>C (GATAD1)
XR_002956474.1:n.2286-1879T>C (GATAD1)
XR_242246.5:n.3738A>G (PEX1)
XR_927494.3:n.1063-1879T>C (GATAD1)
XR_927500.3:n.1060-1879T>C (GATAD1)
XR_927503.3:n.994-1879T>C (GATAD1)
NM_000466.3:c.3696A>G (PEX1) MANE Select	NP_000457.1:p.Ser1232=
NM_001282677.2:c.3525A>G (PEX1)	NP_001269606.1:p.Ser1175=
NM_001282678.2:c.3072A>G (PEX1)	NP_001269607.1:p.Ser1024=