Canonical Allele Identifier: CA456479523

Gene: PEX1 GATAD1

Linked Data

• ClinVar Variation Id: 3053501
• ClinVar RCV Id: RCV003964061
• gnomAD v4: 7-92489385-G-T
• MyVariant Identifiers: chr7:g.92118699G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92489385G>T , CM000669.2:g.92489385G>T	GRCh38
NC_000007.13:g.92118699G>T , CM000669.1:g.92118699G>T	GRCh37
NC_000007.12:g.91956635G>T	NCBI36
NG_008341.1:g.44147C>A
NG_008341.2:g.44147C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.3675C>A (PEX1) MANE Select	ENSP00000248633.4:p.Thr1225=
ENST00000248633.8:c.3675C>A (PEX1)	ENSP00000248633.4:p.Thr1225=
ENST00000428214.5:c.3504C>A (PEX1)	ENSP00000394413.1:p.Thr1168=
ENST00000438045.5:c.2709C>A (PEX1)	ENSP00000410438.1:p.Thr903=
ENST00000469417.1:n.572C>A (PEX1)
ENST00000477342.1:n.410C>A (PEX1)
ENST00000484913.5:n.3714C>A (PEX1)
ENST00000496420.5:n.4725C>A (PEX1)
NM_000466.2:c.3675C>A (PEX1)	NP_000457.1:p.Thr1225=
NM_001282677.1:c.3504C>A (PEX1)	NP_001269606.1:p.Thr1168=
NM_001282678.1:c.3051C>A (PEX1)	NP_001269607.1:p.Thr1017=
XM_005250433.3:c.1926C>A (PEX1)	XP_005250490.1:p.Thr642=
XR_242246.3:n.3766C>A (PEX1)
XR_927494.1:n.1036-1858G>T (GATAD1)
XR_927495.1:n.1036-701G>T (GATAD1)
XR_927496.1:n.1041-1858G>T (GATAD1)
XR_927497.1:n.1036-701G>T (GATAD1)
XR_927498.1:n.1124-1858G>T (GATAD1)
XR_927500.1:n.1033-1858G>T (GATAD1)
XR_927502.1:n.1033-701G>T (GATAD1)
XR_927503.1:n.967-1858G>T (GATAD1)
XM_017012319.2:c.1926C>A (PEX1)	XP_016867808.1:p.Thr642=
XR_001744808.2:n.2697C>A (PEX1)
XR_001744842.2:n.2281-1858G>T (GATAD1)
XR_001744843.2:n.2212-1858G>T (GATAD1)
XR_002956472.1:n.2281-701G>T (GATAD1)
XR_002956473.1:n.2369-1858G>T (GATAD1)
XR_002956474.1:n.2286-1858G>T (GATAD1)
XR_242246.5:n.3717C>A (PEX1)
XR_927494.3:n.1063-1858G>T (GATAD1)
XR_927500.3:n.1060-1858G>T (GATAD1)
XR_927503.3:n.994-1858G>T (GATAD1)
NM_000466.3:c.3675C>A (PEX1) MANE Select	NP_000457.1:p.Thr1225=
NM_001282677.2:c.3504C>A (PEX1)	NP_001269606.1:p.Thr1168=
NM_001282678.2:c.3051C>A (PEX1)	NP_001269607.1:p.Thr1017=