Canonical Allele Identifier: CA4341312

Gene: PEX1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92507055C>T , CM000669.2:g.92507055C>T	GRCh38
NC_000007.13:g.92136369C>T , CM000669.1:g.92136369C>T	GRCh37
NC_000007.12:g.91974305C>T	NCBI36
NG_008341.1:g.26477G>A
NG_008341.2:g.26477G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1742G>A MANE Select	ENSP00000248633.4:p.Arg581Gln
ENST00000248633.8:c.1742G>A	ENSP00000248633.4:p.Arg581Gln
ENST00000422866.1:c.560G>A
ENST00000428214.5:c.1742G>A	ENSP00000394413.1:p.Arg581Gln
ENST00000438045.5:c.776G>A	ENSP00000410438.1:p.Arg259Gln
ENST00000484913.5:n.1781G>A
ENST00000496420.5:n.769G>A
NM_000466.2:c.1742G>A	NP_000457.1:p.Arg581Gln
NM_001282677.1:c.1742G>A	NP_001269606.1:p.Arg581Gln
NM_001282678.1:c.1118G>A	NP_001269607.1:p.Arg373Gln
XM_005250433.3:c.-8G>A	XP_005250490.1:n.-8G>A
XR_242246.3:n.1838G>A
XM_017012319.2:c.-8G>A	XP_016867808.1:n.-8G>A
XR_001744808.2:n.769G>A
XR_242246.5:n.1789G>A
NM_000466.3:c.1742G>A MANE Select	NP_000457.1:p.Arg581Gln
NM_001282677.2:c.1742G>A	NP_001269606.1:p.Arg581Gln
NM_001282678.2:c.1118G>A	NP_001269607.1:p.Arg373Gln