Canonical Allele Identifier: CA2683721003

Gene: PEX1

Linked Data

• dbSNP Id: rs2116252680
• gnomAD v4: 7-92518922-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518922A>G , CM000669.2:g.92518922A>G	GRCh38
NC_000007.13:g.92148236A>G , CM000669.1:g.92148236A>G	GRCh37
NC_000007.12:g.91986172A>G	NCBI36
NG_008341.1:g.14610T>C
NG_008341.2:g.14610T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.357+73T>C MANE Select	ENSP00000248633.4:n.357+73T>C
ENST00000248633.8:c.357+73T>C	ENSP00000248633.4:n.357+73T>C
ENST00000428214.5:c.357+73T>C	ENSP00000394413.1:n.357+73T>C
ENST00000438045.5:c.273+3180T>C	ENSP00000410438.1:n.273+3180T>C
ENST00000484913.5:n.396+38T>C
NM_000466.2:c.357+73T>C	NP_000457.1:n.357+73T>C
NM_001282677.1:c.357+73T>C	NP_001269606.1:n.357+73T>C
NM_001282678.1:c.-268+38T>C	NP_001269607.1:n.-268+38T>C
XR_242246.3:n.453+73T>C
XR_242246.5:n.404+73T>C
NM_000466.3:c.357+73T>C MANE Select	NP_000457.1:n.357+73T>C
NM_001282677.2:c.357+73T>C	NP_001269606.1:n.357+73T>C
NM_001282678.2:c.-268+38T>C	NP_001269607.1:n.-268+38T>C