Canonical Allele Identifier: CA368178863
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92502078T>A , CM000669.2:g.92502078T>A GRCh38
NC_000007.13:g.92131392T>A , CM000669.1:g.92131392T>A GRCh37
NC_000007.12:g.91969328T>A NCBI36
NG_008341.1:g.31454A>T
NG_008341.2:g.31454A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2228A>T MANE Select ENSP00000248633.4:p.Glu743Val
ENST00000248633.8:c.2228A>T ENSP00000248633.4:p.Glu743Val
ENST00000428214.5:c.2057A>T ENSP00000394413.1:p.Glu686Val
ENST00000438045.5:c.1262A>T ENSP00000410438.1:p.Glu421Val
ENST00000484913.5:n.2267A>T
ENST00000496092.1:n.26A>T
ENST00000496420.5:n.1904A>T
NM_000466.2:c.2228A>T NP_000457.1:p.Glu743Val
NM_001282677.1:c.2057A>T NP_001269606.1:p.Glu686Val
NM_001282678.1:c.1604A>T NP_001269607.1:p.Glu535Val
XM_005250433.3:c.479A>T XP_005250490.1:p.Glu160Val
XR_242246.3:n.2324A>T
XM_017012319.2:c.479A>T XP_016867808.1:p.Glu160Val
XR_001744808.2:n.1255A>T
XR_242246.5:n.2275A>T
NM_000466.3:c.2228A>T MANE Select NP_000457.1:p.Glu743Val
NM_001282677.2:c.2057A>T NP_001269606.1:p.Glu686Val
NM_001282678.2:c.1604A>T NP_001269607.1:p.Glu535Val