Canonical Allele Identifier: CA4341581

Gene: PEX1

Linked Data

• dbSNP Id: rs768428948
• ExAC: 7:92147303 G / C
• gnomAD v2: 7-92147303-G-C
• gnomAD v4: 7-92517989-G-C
• MyVariant Identifiers: chr7:g.92147303G>C (hg19) ; chr7:g.92517989G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517989G>C , CM000669.2:g.92517989G>C	GRCh38
NC_000007.13:g.92147303G>C , CM000669.1:g.92147303G>C	GRCh37
NC_000007.12:g.91985239G>C	NCBI36
NG_008341.1:g.15543C>G
NG_008341.2:g.15543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.526C>G MANE Select	ENSP00000248633.4:p.Leu176Val
ENST00000248633.8:c.526C>G	ENSP00000248633.4:p.Leu176Val
ENST00000428214.5:c.526C>G	ENSP00000394413.1:p.Leu176Val
ENST00000438045.5:c.274-4022C>G	ENSP00000410438.1:n.274-4022C>G
ENST00000484913.5:n.565C>G
NM_000466.2:c.526C>G	NP_000457.1:p.Leu176Val
NM_001282677.1:c.526C>G	NP_001269606.1:p.Leu176Val
NM_001282678.1:c.-99C>G	NP_001269607.1:n.-99C>G
XR_242246.3:n.622C>G
XR_242246.5:n.573C>G
NM_000466.3:c.526C>G MANE Select	NP_000457.1:p.Leu176Val
NM_001282677.2:c.526C>G	NP_001269606.1:p.Leu176Val
NM_001282678.2:c.-99C>G	NP_001269607.1:n.-99C>G