Canonical Allele Identifier: CA576305533

Gene: PEX1

Linked Data

• dbSNP Id: rs1213196397
• gnomAD v2: 7-92135533-A-T
• gnomAD v4: 7-92506219-A-T
• MyVariant Identifiers: chr7:g.92135533A>T (hg19) ; chr7:g.92506219A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92506219A>T , CM000669.2:g.92506219A>T	GRCh38
NC_000007.13:g.92135533A>T , CM000669.1:g.92135533A>T	GRCh37
NC_000007.12:g.91973469A>T	NCBI36
NG_008341.1:g.27313T>A
NG_008341.2:g.27313T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1900+29T>A MANE Select	ENSP00000248633.4:n.1900+29T>A
ENST00000248633.8:c.1900+29T>A	ENSP00000248633.4:n.1900+29T>A
ENST00000422866.1:c.718+29T>A
ENST00000428214.5:c.1900+29T>A	ENSP00000394413.1:n.1900+29T>A
ENST00000438045.5:c.934+29T>A	ENSP00000410438.1:n.934+29T>A
ENST00000484913.5:n.1939+29T>A
ENST00000496420.5:n.1576+29T>A
NM_000466.2:c.1900+29T>A	NP_000457.1:n.1900+29T>A
NM_001282677.1:c.1900+29T>A	NP_001269606.1:n.1900+29T>A
NM_001282678.1:c.1276+29T>A	NP_001269607.1:n.1276+29T>A
XM_005250433.3:c.151+29T>A	XP_005250490.1:n.151+29T>A
XR_242246.3:n.1996+29T>A
XM_017012319.2:c.151+29T>A	XP_016867808.1:n.151+29T>A
XR_001744808.2:n.927+29T>A
XR_242246.5:n.1947+29T>A
NM_000466.3:c.1900+29T>A MANE Select	NP_000457.1:n.1900+29T>A
NM_001282677.2:c.1900+29T>A	NP_001269606.1:n.1900+29T>A
NM_001282678.2:c.1276+29T>A	NP_001269607.1:n.1276+29T>A