Canonical Allele Identifier: CA456624533

Gene: PEX1

Linked Data

• dbSNP Id: rs1261529468
• gnomAD v2: 7-92147343-T-A
• gnomAD v4: 7-92518029-T-A
• MyVariant Identifiers: chr7:g.92147343T>A (hg19) ; chr7:g.92518029T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518029T>A , CM000669.2:g.92518029T>A	GRCh38
NC_000007.13:g.92147343T>A , CM000669.1:g.92147343T>A	GRCh37
NC_000007.12:g.91985279T>A	NCBI36
NG_008341.1:g.15503A>T
NG_008341.2:g.15503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.486A>T MANE Select	ENSP00000248633.4:p.Pro162=
ENST00000248633.8:c.486A>T	ENSP00000248633.4:p.Pro162=
ENST00000428214.5:c.486A>T	ENSP00000394413.1:p.Pro162=
ENST00000438045.5:c.274-4062A>T	ENSP00000410438.1:n.274-4062A>T
ENST00000484913.5:n.525A>T
NM_000466.2:c.486A>T	NP_000457.1:p.Pro162=
NM_001282677.1:c.486A>T	NP_001269606.1:p.Pro162=
NM_001282678.1:c.-139A>T	NP_001269607.1:n.-139A>T
XR_242246.3:n.582A>T
XR_242246.5:n.533A>T
NM_000466.3:c.486A>T MANE Select	NP_000457.1:p.Pro162=
NM_001282677.2:c.486A>T	NP_001269606.1:p.Pro162=
NM_001282678.2:c.-139A>T	NP_001269607.1:n.-139A>T