Canonical Allele Identifier: CA368201311

Gene: PEX1

Linked Data

• ClinVar Variation Id: 805118
• ClinVar RCV Id: RCV000992521
• dbSNP Id: rs149806989
• MyVariant Identifiers: chr7:g.92147282G>C (hg19) ; chr7:g.92517968G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517968G>C , CM000669.2:g.92517968G>C	GRCh38
NC_000007.13:g.92147282G>C , CM000669.1:g.92147282G>C	GRCh37
NC_000007.12:g.91985218G>C	NCBI36
NG_008341.1:g.15564C>G
NG_008341.2:g.15564C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.547C>G MANE Select	ENSP00000248633.4:p.Arg183Gly
ENST00000248633.8:c.547C>G	ENSP00000248633.4:p.Arg183Gly
ENST00000428214.5:c.547C>G	ENSP00000394413.1:p.Arg183Gly
ENST00000438045.5:c.274-4001C>G	ENSP00000410438.1:n.274-4001C>G
ENST00000484913.5:n.586C>G
NM_000466.2:c.547C>G	NP_000457.1:p.Arg183Gly
NM_001282677.1:c.547C>G	NP_001269606.1:p.Arg183Gly
NM_001282678.1:c.-78C>G	NP_001269607.1:n.-78C>G
XR_242246.3:n.643C>G
XR_242246.5:n.594C>G
NM_000466.3:c.547C>G MANE Select	NP_000457.1:p.Arg183Gly
NM_001282677.2:c.547C>G	NP_001269606.1:p.Arg183Gly
NM_001282678.2:c.-78C>G	NP_001269607.1:n.-78C>G