Canonical Allele Identifier: CA2578938279
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518875T>C , CM000669.2:g.92518875T>C GRCh38
NC_000007.13:g.92148189T>C , CM000669.1:g.92148189T>C GRCh37
NC_000007.12:g.91986125T>C NCBI36
NG_008341.1:g.14657A>G
NG_008341.2:g.14657A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.357+120A>G MANE Select ENSP00000248633.4:n.357+120A>G
ENST00000248633.8:c.357+120A>G ENSP00000248633.4:n.357+120A>G
ENST00000428214.5:c.357+120A>G ENSP00000394413.1:n.357+120A>G
ENST00000438045.5:c.273+3227A>G ENSP00000410438.1:n.273+3227A>G
ENST00000484913.5:n.396+85A>G
NM_000466.2:c.357+120A>G NP_000457.1:n.357+120A>G
NM_001282677.1:c.357+120A>G NP_001269606.1:n.357+120A>G
NM_001282678.1:c.-268+85A>G NP_001269607.1:n.-268+85A>G
XR_242246.3:n.453+120A>G
XR_242246.5:n.404+120A>G
NM_000466.3:c.357+120A>G MANE Select NP_000457.1:n.357+120A>G
NM_001282677.2:c.357+120A>G NP_001269606.1:n.357+120A>G
NM_001282678.2:c.-268+85A>G NP_001269607.1:n.-268+85A>G