Canonical Allele Identifier: CA2683721228

Gene: PEX1

Linked Data

• gnomAD v4: 7-92521984-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92521984A>G , CM000669.2:g.92521984A>G	GRCh38
NC_000007.13:g.92151298A>G , CM000669.1:g.92151298A>G	GRCh37
NC_000007.12:g.91989234A>G	NCBI36
NG_008341.1:g.11548T>C
NG_008341.2:g.11548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.273+118T>C MANE Select	ENSP00000248633.4:n.273+118T>C
ENST00000248633.8:c.273+118T>C	ENSP00000248633.4:n.273+118T>C
ENST00000428214.5:c.273+118T>C	ENSP00000394413.1:n.273+118T>C
ENST00000438045.5:c.273+118T>C	ENSP00000410438.1:n.273+118T>C
ENST00000484913.5:n.277+118T>C
NM_000466.2:c.273+118T>C	NP_000457.1:n.273+118T>C
NM_001282677.1:c.273+118T>C	NP_001269606.1:n.273+118T>C
NM_001282678.1:c.-387+118T>C	NP_001269607.1:n.-387+118T>C
XR_242246.3:n.369+118T>C
XR_242246.5:n.320+118T>C
NM_000466.3:c.273+118T>C MANE Select	NP_000457.1:n.273+118T>C
NM_001282677.2:c.273+118T>C	NP_001269606.1:n.273+118T>C
NM_001282678.2:c.-387+118T>C	NP_001269607.1:n.-387+118T>C