Canonical Allele Identifier: CA161973191

Gene: PEX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92517276C>T , CM000669.2:g.92517276C>T	GRCh38
NC_000007.13:g.92146590C>T , CM000669.1:g.92146590C>T	GRCh37
NC_000007.12:g.91984526C>T	NCBI36
NG_008341.1:g.16256G>A
NG_008341.2:g.16256G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000466.3:c.1239G>A MANE Select	NP_000457.1:p.Trp413Ter
ENST00000248633.9:c.1239G>A MANE Select	ENSP00000248633.4:p.Trp413Ter
NM_000466.2:c.1239G>A	NP_000457.1:p.Trp413Ter
NM_001282677.1:c.1239G>A	NP_001269606.1:p.Trp413Ter
NM_001282677.2:c.1239G>A	NP_001269606.1:p.Trp413Ter
NM_001282678.1:c.615G>A	NP_001269607.1:p.Trp205Ter
NM_001282678.2:c.615G>A	NP_001269607.1:p.Trp205Ter
ENST00000248633.8:c.1239G>A	ENSP00000248633.4:p.Trp413Ter
ENST00000422866.1:c.140G>A
ENST00000428214.5:c.1239G>A	ENSP00000394413.1:p.Trp413Ter
ENST00000438045.5:c.274-3309G>A	ENSP00000410438.1:n.274-3309G>A
ENST00000484913.5:n.1278G>A
XM_017012319.2:c.-428G>A	XP_016867808.1:n.-428G>A
XR_001744808.2:n.349G>A
XR_242246.3:n.1335G>A
XR_242246.5:n.1286G>A