Canonical Allele Identifier: CA2580077827

Gene: PEX1

Linked Data

• ClinVar Variation Id: 2094418
• ClinVar RCV Id: RCV003010278

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506238A>G , CM000669.2:g.92506238A>G	GRCh38
NC_000007.13:g.92135552A>G , CM000669.1:g.92135552A>G	GRCh37
NC_000007.12:g.91973488A>G	NCBI36
NG_008341.1:g.27294T>C
NG_008341.2:g.27294T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1900+10T>C MANE Select	ENSP00000248633.4:n.1900+10T>C
ENST00000248633.8:c.1900+10T>C	ENSP00000248633.4:n.1900+10T>C
ENST00000422866.1:c.718+10T>C
ENST00000428214.5:c.1900+10T>C	ENSP00000394413.1:n.1900+10T>C
ENST00000438045.5:c.934+10T>C	ENSP00000410438.1:n.934+10T>C
ENST00000484913.5:n.1939+10T>C
ENST00000496420.5:n.1576+10T>C
NM_000466.2:c.1900+10T>C	NP_000457.1:n.1900+10T>C
NM_001282677.1:c.1900+10T>C	NP_001269606.1:n.1900+10T>C
NM_001282678.1:c.1276+10T>C	NP_001269607.1:n.1276+10T>C
XM_005250433.3:c.151+10T>C	XP_005250490.1:n.151+10T>C
XR_242246.3:n.1996+10T>C
XM_017012319.2:c.151+10T>C	XP_016867808.1:n.151+10T>C
XR_001744808.2:n.927+10T>C
XR_242246.5:n.1947+10T>C
NM_000466.3:c.1900+10T>C MANE Select	NP_000457.1:n.1900+10T>C
NM_001282677.2:c.1900+10T>C	NP_001269606.1:n.1900+10T>C
NM_001282678.2:c.1276+10T>C	NP_001269607.1:n.1276+10T>C