Canonical Allele Identifier: CA2683720486

Gene: PEX1

Linked Data

• gnomAD v4: 7-92510939-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510941dup , CM000669.2:g.92510941dup	GRCh38
NC_000007.13:g.92140255dup , CM000669.1:g.92140255dup	GRCh37
NC_000007.12:g.91978191dup	NCBI36
NG_008341.1:g.22592dup
NG_008341.2:g.22592dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1587+4dup MANE Select	ENSP00000248633.4:n.1587+4dup
ENST00000248633.8:c.1587+4dup	ENSP00000248633.4:n.1587+4dup
ENST00000422866.1:c.488+4dup
ENST00000428214.5:c.1587+4dup	ENSP00000394413.1:n.1587+4dup
ENST00000438045.5:c.621+4dup	ENSP00000410438.1:n.621+4dup
ENST00000476923.1:n.352dup
ENST00000484913.5:n.1626+4dup
NM_000466.2:c.1587+4dup	NP_000457.1:n.1587+4dup
NM_001282677.1:c.1587+4dup	NP_001269606.1:n.1587+4dup
NM_001282678.1:c.963+4dup	NP_001269607.1:n.963+4dup
XM_005250433.3:c.-80+4dup	XP_005250490.1:n.-80+4dup
XR_242246.3:n.1683+4dup
XM_017012319.2:c.-80+4dup	XP_016867808.1:n.-80+4dup
XR_001744808.2:n.697+4dup
XR_242246.5:n.1634+4dup
NM_000466.3:c.1587+4dup MANE Select	NP_000457.1:n.1587+4dup
NM_001282677.2:c.1587+4dup	NP_001269606.1:n.1587+4dup
NM_001282678.2:c.963+4dup	NP_001269607.1:n.963+4dup