Canonical Allele Identifier: CA368190315

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92511024T>G , CM000669.2:g.92511024T>G	GRCh38
NC_000007.13:g.92140338T>G , CM000669.1:g.92140338T>G	GRCh37
NC_000007.12:g.91978274T>G	NCBI36
NG_008341.1:g.22508A>C
NG_008341.2:g.22508A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1507A>C MANE Select	ENSP00000248633.4:p.Ile503Leu
ENST00000248633.8:c.1507A>C	ENSP00000248633.4:p.Ile503Leu
ENST00000422866.1:c.408A>C
ENST00000428214.5:c.1507A>C	ENSP00000394413.1:p.Ile503Leu
ENST00000438045.5:c.541A>C	ENSP00000410438.1:p.Ile181Leu
ENST00000476923.1:n.268A>C
ENST00000484913.5:n.1546A>C
NM_000466.2:c.1507A>C	NP_000457.1:p.Ile503Leu
NM_001282677.1:c.1507A>C	NP_001269606.1:p.Ile503Leu
NM_001282678.1:c.883A>C	NP_001269607.1:p.Ile295Leu
XM_005250433.3:c.-160A>C	XP_005250490.1:n.-160A>C
XR_242246.3:n.1603A>C
XM_017012319.2:c.-160A>C	XP_016867808.1:n.-160A>C
XR_001744808.2:n.617A>C
XR_242246.5:n.1554A>C
NM_000466.3:c.1507A>C MANE Select	NP_000457.1:p.Ile503Leu
NM_001282677.2:c.1507A>C	NP_001269606.1:p.Ile503Leu
NM_001282678.2:c.883A>C	NP_001269607.1:p.Ile295Leu