Canonical Allele Identifier: CA368202069
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518156T>G , CM000669.2:g.92518156T>G GRCh38
NC_000007.13:g.92147470T>G , CM000669.1:g.92147470T>G GRCh37
NC_000007.12:g.91985406T>G NCBI36
NG_008341.1:g.15376A>C
NG_008341.2:g.15376A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.457A>C MANE Select ENSP00000248633.4:p.Ile153Leu
ENST00000248633.8:c.457A>C ENSP00000248633.4:p.Ile153Leu
ENST00000428214.5:c.457A>C ENSP00000394413.1:p.Ile153Leu
ENST00000438045.5:c.273+3946A>C ENSP00000410438.1:n.273+3946A>C
ENST00000484913.5:n.496A>C
NM_000466.2:c.457A>C NP_000457.1:p.Ile153Leu
NM_001282677.1:c.457A>C NP_001269606.1:p.Ile153Leu
NM_001282678.1:c.-168A>C NP_001269607.1:n.-168A>C
XR_242246.3:n.553A>C
XR_242246.5:n.504A>C
NM_000466.3:c.457A>C MANE Select NP_000457.1:p.Ile153Leu
NM_001282677.2:c.457A>C NP_001269606.1:p.Ile153Leu
NM_001282678.2:c.-168A>C NP_001269607.1:n.-168A>C