Canonical Allele Identifier: CA368183868

Gene: PEX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92504854T>G , CM000669.2:g.92504854T>G	GRCh38
NC_000007.13:g.92134168T>G , CM000669.1:g.92134168T>G	GRCh37
NC_000007.12:g.91972104T>G	NCBI36
NG_008341.1:g.28678A>C
NG_008341.2:g.28678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.1949A>C MANE Select	ENSP00000248633.4:p.Glu650Ala
ENST00000248633.8:c.1949A>C	ENSP00000248633.4:p.Glu650Ala
ENST00000428214.5:c.1900+1394A>C	ENSP00000394413.1:n.1900+1394A>C
ENST00000438045.5:c.983A>C	ENSP00000410438.1:p.Glu328Ala
ENST00000484913.5:n.1988A>C
ENST00000496420.5:n.1625A>C
NM_000466.2:c.1949A>C	NP_000457.1:p.Glu650Ala
NM_001282677.1:c.1900+1394A>C	NP_001269606.1:n.1900+1394A>C
NM_001282678.1:c.1325A>C	NP_001269607.1:p.Glu442Ala
XM_005250433.3:c.200A>C	XP_005250490.1:p.Glu67Ala
XR_242246.3:n.2045A>C
XM_017012319.2:c.200A>C	XP_016867808.1:p.Glu67Ala
XR_001744808.2:n.976A>C
XR_242246.5:n.1996A>C
NM_000466.3:c.1949A>C MANE Select	NP_000457.1:p.Glu650Ala
NM_001282677.2:c.1900+1394A>C	NP_001269606.1:n.1900+1394A>C
NM_001282678.2:c.1325A>C	NP_001269607.1:p.Glu442Ala