Canonical Allele Identifier: CA368203343

Gene: PEX1

Linked Data

• gnomAD v4: 7-92519075-A-T
• MyVariant Identifiers: chr7:g.92148389A>T (hg19) ; chr7:g.92519075A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92519075A>T , CM000669.2:g.92519075A>T	GRCh38
NC_000007.13:g.92148389A>T , CM000669.1:g.92148389A>T	GRCh37
NC_000007.12:g.91986325A>T	NCBI36
NG_008341.1:g.14457T>A
NG_008341.2:g.14457T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.277T>A MANE Select	ENSP00000248633.4:p.Phe93Ile
ENST00000248633.8:c.277T>A	ENSP00000248633.4:p.Phe93Ile
ENST00000428214.5:c.277T>A	ENSP00000394413.1:p.Phe93Ile
ENST00000438045.5:c.273+3027T>A	ENSP00000410438.1:n.273+3027T>A
ENST00000484913.5:n.281T>A
NM_000466.2:c.277T>A	NP_000457.1:p.Phe93Ile
NM_001282677.1:c.277T>A	NP_001269606.1:p.Phe93Ile
NM_001282678.1:c.-383T>A	NP_001269607.1:n.-383T>A
XR_242246.3:n.373T>A
XR_242246.5:n.324T>A
NM_000466.3:c.277T>A MANE Select	NP_000457.1:p.Phe93Ile
NM_001282677.2:c.277T>A	NP_001269606.1:p.Phe93Ile
NM_001282678.2:c.-383T>A	NP_001269607.1:n.-383T>A