Canonical Allele Identifier: CA1725951767

Gene: PEX1

Linked Data

• dbSNP Id: rs1793088574

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92522351T>C , CM000669.2:g.92522351T>C	GRCh38
NC_000007.13:g.92151665T>C , CM000669.1:g.92151665T>C	GRCh37
NC_000007.12:g.91989601T>C	NCBI36
NG_008341.1:g.11181A>G
NG_008341.2:g.11181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.130-106A>G MANE Select	ENSP00000248633.4:n.130-106A>G
ENST00000248633.8:c.130-106A>G	ENSP00000248633.4:n.130-106A>G
ENST00000428214.5:c.130-106A>G	ENSP00000394413.1:n.130-106A>G
ENST00000438045.5:c.130-106A>G	ENSP00000410438.1:n.130-106A>G
ENST00000484913.5:n.134-106A>G
NM_000466.2:c.130-106A>G	NP_000457.1:n.130-106A>G
NM_001282677.1:c.130-106A>G	NP_001269606.1:n.130-106A>G
NM_001282678.1:c.-530-106A>G	NP_001269607.1:n.-530-106A>G
XR_242246.3:n.226-106A>G
XR_242246.5:n.177-106A>G
NM_000466.3:c.130-106A>G MANE Select	NP_000457.1:n.130-106A>G
NM_001282677.2:c.130-106A>G	NP_001269606.1:n.130-106A>G
NM_001282678.2:c.-530-106A>G	NP_001269607.1:n.-530-106A>G