Canonical Allele Identifier: CA2683720592

Gene: PEX1

Linked Data

• gnomAD v4: 7-92518068-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518068T>G , CM000669.2:g.92518068T>G	GRCh38
NC_000007.13:g.92147382T>G , CM000669.1:g.92147382T>G	GRCh37
NC_000007.12:g.91985318T>G	NCBI36
NG_008341.1:g.15464A>C
NG_008341.2:g.15464A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.473-26A>C MANE Select	ENSP00000248633.4:n.473-26A>C
ENST00000248633.8:c.473-26A>C	ENSP00000248633.4:n.473-26A>C
ENST00000428214.5:c.473-26A>C	ENSP00000394413.1:n.473-26A>C
ENST00000438045.5:c.273+4034A>C	ENSP00000410438.1:n.273+4034A>C
ENST00000484913.5:n.512-26A>C
NM_000466.2:c.473-26A>C	NP_000457.1:n.473-26A>C
NM_001282677.1:c.473-26A>C	NP_001269606.1:n.473-26A>C
NM_001282678.1:c.-152-26A>C	NP_001269607.1:n.-152-26A>C
XR_242246.3:n.569-26A>C
XR_242246.5:n.520-26A>C
NM_000466.3:c.473-26A>C MANE Select	NP_000457.1:n.473-26A>C
NM_001282677.2:c.473-26A>C	NP_001269606.1:n.473-26A>C
NM_001282678.2:c.-152-26A>C	NP_001269607.1:n.-152-26A>C