Canonical Allele Identifier: CA368197204

Gene: PEX1

Linked Data

• dbSNP Id: rs1792834655
• gnomAD v3: 7-92517313-G-T
• gnomAD v4: 7-92517313-G-T
• MyVariant Identifiers: chr7:g.92146627G>T (hg19) ; chr7:g.92517313G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517313G>T , CM000669.2:g.92517313G>T	GRCh38
NC_000007.13:g.92146627G>T , CM000669.1:g.92146627G>T	GRCh37
NC_000007.12:g.91984563G>T	NCBI36
NG_008341.1:g.16219C>A
NG_008341.2:g.16219C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1202C>A MANE Select	ENSP00000248633.4:p.Thr401Asn
ENST00000248633.8:c.1202C>A	ENSP00000248633.4:p.Thr401Asn
ENST00000422866.1:c.103C>A
ENST00000428214.5:c.1202C>A	ENSP00000394413.1:p.Thr401Asn
ENST00000438045.5:c.274-3346C>A	ENSP00000410438.1:n.274-3346C>A
ENST00000484913.5:n.1241C>A
NM_000466.2:c.1202C>A	NP_000457.1:p.Thr401Asn
NM_001282677.1:c.1202C>A	NP_001269606.1:p.Thr401Asn
NM_001282678.1:c.578C>A	NP_001269607.1:p.Thr193Asn
XR_242246.3:n.1298C>A
XM_017012319.2:c.-465C>A	XP_016867808.1:n.-465C>A
XR_001744808.2:n.312C>A
XR_242246.5:n.1249C>A
NM_000466.3:c.1202C>A MANE Select	NP_000457.1:p.Thr401Asn
NM_001282677.2:c.1202C>A	NP_001269606.1:p.Thr401Asn
NM_001282678.2:c.578C>A	NP_001269607.1:p.Thr193Asn