Canonical Allele Identifier: CA161978946

Gene: PEX1

Linked Data

• ClinVar Variation Id: 2149406
• ClinVar RCV Id: RCV003065464
• dbSNP Id: rs1010885689
• gnomAD v4: 7-92522221-T-C
• MyVariant Identifiers: chr7:g.92151535T>C (hg19) ; chr7:g.92522221T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522221T>C , CM000669.2:g.92522221T>C	GRCh38
NC_000007.13:g.92151535T>C , CM000669.1:g.92151535T>C	GRCh37
NC_000007.12:g.91989471T>C	NCBI36
NG_008341.1:g.11311A>G
NG_008341.2:g.11311A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.154A>G MANE Select	ENSP00000248633.4:p.Ser52Gly
ENST00000248633.8:c.154A>G	ENSP00000248633.4:p.Ser52Gly
ENST00000428214.5:c.154A>G	ENSP00000394413.1:p.Ser52Gly
ENST00000438045.5:c.154A>G	ENSP00000410438.1:p.Ser52Gly
ENST00000484913.5:n.158A>G
NM_000466.2:c.154A>G	NP_000457.1:p.Ser52Gly
NM_001282677.1:c.154A>G	NP_001269606.1:p.Ser52Gly
NM_001282678.1:c.-506A>G	NP_001269607.1:n.-506A>G
XR_242246.3:n.250A>G
XR_242246.5:n.201A>G
NM_000466.3:c.154A>G MANE Select	NP_000457.1:p.Ser52Gly
NM_001282677.2:c.154A>G	NP_001269606.1:p.Ser52Gly
NM_001282678.2:c.-506A>G	NP_001269607.1:n.-506A>G