Canonical Allele Identifier: CA456480444

Gene: PEX1 GATAD1

Linked Data

• dbSNP Id: rs1791175075
• gnomAD v4: 7-92489741-G-A
• MyVariant Identifiers: chr7:g.92119055G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92489741G>A , CM000669.2:g.92489741G>A	GRCh38
NC_000007.13:g.92119055G>A , CM000669.1:g.92119055G>A	GRCh37
NC_000007.12:g.91956991G>A	NCBI36
NG_008341.1:g.43791C>T
NG_008341.2:g.43791C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.3609C>T (PEX1) MANE Select	ENSP00000248633.4:p.Ile1203=
ENST00000248633.8:c.3609C>T (PEX1)	ENSP00000248633.4:p.Ile1203=
ENST00000428214.5:c.3438C>T (PEX1)	ENSP00000394413.1:p.Ile1146=
ENST00000438045.5:c.2643C>T (PEX1)	ENSP00000410438.1:p.Ile881=
ENST00000469417.1:n.506C>T (PEX1)
ENST00000477342.1:n.54C>T (PEX1)
ENST00000484913.5:n.3648C>T (PEX1)
ENST00000496420.5:n.4664C>T (PEX1)
NM_000466.2:c.3609C>T (PEX1)	NP_000457.1:p.Ile1203=
NM_001282677.1:c.3438C>T (PEX1)	NP_001269606.1:p.Ile1146=
NM_001282678.1:c.2985C>T (PEX1)	NP_001269607.1:p.Ile995=
XM_005250433.3:c.1860C>T (PEX1)	XP_005250490.1:p.Ile620=
XR_242246.3:n.3705C>T (PEX1)
XR_927494.1:n.1036-1502G>A (GATAD1)
XR_927495.1:n.1036-345G>A (GATAD1)
XR_927496.1:n.1041-1502G>A (GATAD1)
XR_927497.1:n.1036-345G>A (GATAD1)
XR_927498.1:n.1124-1502G>A (GATAD1)
XR_927500.1:n.1033-1502G>A (GATAD1)
XR_927502.1:n.1033-345G>A (GATAD1)
XR_927503.1:n.967-1502G>A (GATAD1)
XM_017012319.2:c.1860C>T (PEX1)	XP_016867808.1:p.Ile620=
XR_001744808.2:n.2636C>T (PEX1)
XR_001744842.2:n.2281-1502G>A (GATAD1)
XR_001744843.2:n.2212-1502G>A (GATAD1)
XR_002956472.1:n.2281-345G>A (GATAD1)
XR_002956473.1:n.2369-1502G>A (GATAD1)
XR_002956474.1:n.2286-1502G>A (GATAD1)
XR_242246.5:n.3656C>T (PEX1)
XR_927494.3:n.1063-1502G>A (GATAD1)
XR_927500.3:n.1060-1502G>A (GATAD1)
XR_927503.3:n.994-1502G>A (GATAD1)
NM_000466.3:c.3609C>T (PEX1) MANE Select	NP_000457.1:p.Ile1203=
NM_001282677.2:c.3438C>T (PEX1)	NP_001269606.1:p.Ile1146=
NM_001282678.2:c.2985C>T (PEX1)	NP_001269607.1:p.Ile995=