Canonical Allele Identifier: CA161973281

Gene: PEX1

Linked Data

• ClinVar Variation Id: 759212
• ClinVar RCV Id: RCV001277059
• dbSNP Id: rs776933950
• gnomAD v3: 7-92517363-T-C
• gnomAD v4: 7-92517363-T-C
• MyVariant Identifiers: chr7:g.92146677T>C (hg19) ; chr7:g.92517363T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517363T>C , CM000669.2:g.92517363T>C	GRCh38
NC_000007.13:g.92146677T>C , CM000669.1:g.92146677T>C	GRCh37
NC_000007.12:g.91984613T>C	NCBI36
NG_008341.1:g.16169A>G
NG_008341.2:g.16169A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1152A>G MANE Select	ENSP00000248633.4:p.Leu384=
ENST00000248633.8:c.1152A>G	ENSP00000248633.4:p.Leu384=
ENST00000422866.1:c.53A>G
ENST00000428214.5:c.1152A>G	ENSP00000394413.1:p.Leu384=
ENST00000438045.5:c.274-3396A>G	ENSP00000410438.1:n.274-3396A>G
ENST00000484913.5:n.1191A>G
NM_000466.2:c.1152A>G	NP_000457.1:p.Leu384=
NM_001282677.1:c.1152A>G	NP_001269606.1:p.Leu384=
NM_001282678.1:c.528A>G	NP_001269607.1:p.Leu176=
XR_242246.3:n.1248A>G
XM_017012319.2:c.-515A>G	XP_016867808.1:n.-515A>G
XR_001744808.2:n.262A>G
XR_242246.5:n.1199A>G
NM_000466.3:c.1152A>G MANE Select	NP_000457.1:p.Leu384=
NM_001282677.2:c.1152A>G	NP_001269606.1:p.Leu384=
NM_001282678.2:c.528A>G	NP_001269607.1:p.Leu176=