Canonical Allele Identifier: CA456481462

Gene: PEX1 GATAD1

Linked Data

• gnomAD v4: 7-92494353-G-A
• MyVariant Identifiers: chr7:g.92123667G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92494353G>A , CM000669.2:g.92494353G>A	GRCh38
NC_000007.13:g.92123667G>A , CM000669.1:g.92123667G>A	GRCh37
NC_000007.12:g.91961603G>A	NCBI36
NG_008341.1:g.39179C>T
NG_008341.2:g.39179C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.2970C>T (PEX1) MANE Select	ENSP00000248633.4:p.Asp990=
ENST00000248633.8:c.2970C>T (PEX1)	ENSP00000248633.4:p.Asp990=
ENST00000428214.5:c.2799C>T (PEX1)	ENSP00000394413.1:p.Asp933=
ENST00000438045.5:c.2004C>T (PEX1)	ENSP00000410438.1:p.Asp668=
ENST00000484913.5:n.3009C>T (PEX1)
ENST00000496420.5:n.2862C>T (PEX1)
NM_000466.2:c.2970C>T (PEX1)	NP_000457.1:p.Asp990=
NM_001282677.1:c.2799C>T (PEX1)	NP_001269606.1:p.Asp933=
NM_001282678.1:c.2346C>T (PEX1)	NP_001269607.1:p.Asp782=
XM_005250433.3:c.1221C>T (PEX1)	XP_005250490.1:p.Asp407=
XR_242246.3:n.3066C>T (PEX1)
XM_017012319.2:c.1221C>T (PEX1)	XP_016867808.1:p.Asp407=
XR_001744808.2:n.1997C>T (PEX1)
XR_001744843.2:n.5322G>A (GATAD1)
XR_242246.5:n.3017C>T (PEX1)
XR_927494.3:n.4173G>A (GATAD1)
XR_927503.3:n.4104G>A (GATAD1)
NM_000466.3:c.2970C>T (PEX1) MANE Select	NP_000457.1:p.Asp990=
NM_001282677.2:c.2799C>T (PEX1)	NP_001269606.1:p.Asp933=
NM_001282678.2:c.2346C>T (PEX1)	NP_001269607.1:p.Asp782=