Canonical Allele Identifier: CA368202088
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518159A>T , CM000669.2:g.92518159A>T GRCh38
NC_000007.13:g.92147473A>T , CM000669.1:g.92147473A>T GRCh37
NC_000007.12:g.91985409A>T NCBI36
NG_008341.1:g.15373T>A
NG_008341.2:g.15373T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.454T>A MANE Select ENSP00000248633.4:p.Tyr152Asn
ENST00000248633.8:c.454T>A ENSP00000248633.4:p.Tyr152Asn
ENST00000428214.5:c.454T>A ENSP00000394413.1:p.Tyr152Asn
ENST00000438045.5:c.273+3943T>A ENSP00000410438.1:n.273+3943T>A
ENST00000484913.5:n.493T>A
NM_000466.2:c.454T>A NP_000457.1:p.Tyr152Asn
NM_001282677.1:c.454T>A NP_001269606.1:p.Tyr152Asn
NM_001282678.1:c.-171T>A NP_001269607.1:n.-171T>A
XR_242246.3:n.550T>A
XR_242246.5:n.501T>A
NM_000466.3:c.454T>A MANE Select NP_000457.1:p.Tyr152Asn
NM_001282677.2:c.454T>A NP_001269606.1:p.Tyr152Asn
NM_001282678.2:c.-171T>A NP_001269607.1:n.-171T>A