Canonical Allele Identifier: CA2683719085

Gene: PEX1

Linked Data

• gnomAD v4: 7-92506130-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506130A>C , CM000669.2:g.92506130A>C	GRCh38
NC_000007.13:g.92135444A>C , CM000669.1:g.92135444A>C	GRCh37
NC_000007.12:g.91973380A>C	NCBI36
NG_008341.1:g.27402T>G
NG_008341.2:g.27402T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1900+118T>G MANE Select	ENSP00000248633.4:n.1900+118T>G
ENST00000248633.8:c.1900+118T>G	ENSP00000248633.4:n.1900+118T>G
ENST00000422866.1:c.718+118T>G
ENST00000428214.5:c.1900+118T>G	ENSP00000394413.1:n.1900+118T>G
ENST00000438045.5:c.934+118T>G	ENSP00000410438.1:n.934+118T>G
ENST00000484913.5:n.1939+118T>G
ENST00000496420.5:n.1576+118T>G
NM_000466.2:c.1900+118T>G	NP_000457.1:n.1900+118T>G
NM_001282677.1:c.1900+118T>G	NP_001269606.1:n.1900+118T>G
NM_001282678.1:c.1276+118T>G	NP_001269607.1:n.1276+118T>G
XM_005250433.3:c.151+118T>G	XP_005250490.1:n.151+118T>G
XR_242246.3:n.1996+118T>G
XM_017012319.2:c.151+118T>G	XP_016867808.1:n.151+118T>G
XR_001744808.2:n.927+118T>G
XR_242246.5:n.1947+118T>G
NM_000466.3:c.1900+118T>G MANE Select	NP_000457.1:n.1900+118T>G
NM_001282677.2:c.1900+118T>G	NP_001269606.1:n.1900+118T>G
NM_001282678.2:c.1276+118T>G	NP_001269607.1:n.1276+118T>G