Canonical Allele Identifier: CA4341141
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs751131867
gnomAD v2: 7-92131230-G-A
gnomAD v4: 7-92501916-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92501916G>A , CM000669.2:g.92501916G>A GRCh38
NC_000007.13:g.92131230G>A , CM000669.1:g.92131230G>A GRCh37
NC_000007.12:g.91969166G>A NCBI36
NG_008341.1:g.31616C>T
NG_008341.2:g.31616C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2390C>T MANE Select ENSP00000248633.4:p.Ser797Phe
ENST00000248633.8:c.2390C>T ENSP00000248633.4:p.Ser797Phe
ENST00000428214.5:c.2219C>T ENSP00000394413.1:p.Ser740Phe
ENST00000438045.5:c.1424C>T ENSP00000410438.1:p.Ser475Phe
ENST00000484913.5:n.2429C>T
ENST00000496092.1:n.188C>T
ENST00000496420.5:n.2066C>T
NM_000466.2:c.2390C>T NP_000457.1:p.Ser797Phe
NM_001282677.1:c.2219C>T NP_001269606.1:p.Ser740Phe
NM_001282678.1:c.1766C>T NP_001269607.1:p.Ser589Phe
XM_005250433.3:c.641C>T XP_005250490.1:p.Ser214Phe
XR_242246.3:n.2486C>T
XM_017012319.2:c.641C>T XP_016867808.1:p.Ser214Phe
XR_001744808.2:n.1417C>T
XR_242246.5:n.2437C>T
NM_000466.3:c.2390C>T MANE Select NP_000457.1:p.Ser797Phe
NM_001282677.2:c.2219C>T NP_001269606.1:p.Ser740Phe
NM_001282678.2:c.1766C>T NP_001269607.1:p.Ser589Phe