Canonical Allele Identifier: CA1725949079

Gene: PEX1

Linked Data

• dbSNP Id: rs1395590289

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92518784G>A , CM000669.2:g.92518784G>A	GRCh38
NC_000007.13:g.92148098G>A , CM000669.1:g.92148098G>A	GRCh37
NC_000007.12:g.91986034G>A	NCBI36
NG_008341.1:g.14748C>T
NG_008341.2:g.14748C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248633.9:c.357+211C>T MANE Select	ENSP00000248633.4:n.357+211C>T
ENST00000248633.8:c.357+211C>T	ENSP00000248633.4:n.357+211C>T
ENST00000428214.5:c.357+211C>T	ENSP00000394413.1:n.357+211C>T
ENST00000438045.5:c.273+3318C>T	ENSP00000410438.1:n.273+3318C>T
ENST00000484913.5:n.396+176C>T
NM_000466.2:c.357+211C>T	NP_000457.1:n.357+211C>T
NM_001282677.1:c.357+211C>T	NP_001269606.1:n.357+211C>T
NM_001282678.1:c.-268+176C>T	NP_001269607.1:n.-268+176C>T
XR_242246.3:n.453+211C>T
XR_242246.5:n.404+211C>T
NM_000466.3:c.357+211C>T MANE Select	NP_000457.1:n.357+211C>T
NM_001282677.2:c.357+211C>T	NP_001269606.1:n.357+211C>T
NM_001282678.2:c.-268+176C>T	NP_001269607.1:n.-268+176C>T