Canonical Allele Identifier: CA2683720452

Gene: PEX1

Linked Data

• gnomAD v4: 7-92510833-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92510833C>T , CM000669.2:g.92510833C>T	GRCh38
NC_000007.13:g.92140147C>T , CM000669.1:g.92140147C>T	GRCh37
NC_000007.12:g.91978083C>T	NCBI36
NG_008341.1:g.22699G>A
NG_008341.2:g.22699G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000248633.9:c.1587+111G>A MANE Select	ENSP00000248633.4:n.1587+111G>A
ENST00000248633.8:c.1587+111G>A	ENSP00000248633.4:n.1587+111G>A
ENST00000422866.1:c.488+111G>A
ENST00000428214.5:c.1587+111G>A	ENSP00000394413.1:n.1587+111G>A
ENST00000438045.5:c.621+111G>A	ENSP00000410438.1:n.621+111G>A
ENST00000484913.5:n.1626+111G>A
NM_000466.2:c.1587+111G>A	NP_000457.1:n.1587+111G>A
NM_001282677.1:c.1587+111G>A	NP_001269606.1:n.1587+111G>A
NM_001282678.1:c.963+111G>A	NP_001269607.1:n.963+111G>A
XM_005250433.3:c.-80+111G>A	XP_005250490.1:n.-80+111G>A
XR_242246.3:n.1683+111G>A
XM_017012319.2:c.-80+111G>A	XP_016867808.1:n.-80+111G>A
XR_001744808.2:n.697+111G>A
XR_242246.5:n.1634+111G>A
NM_000466.3:c.1587+111G>A MANE Select	NP_000457.1:n.1587+111G>A
NM_001282677.2:c.1587+111G>A	NP_001269606.1:n.1587+111G>A
NM_001282678.2:c.963+111G>A	NP_001269607.1:n.963+111G>A