Canonical Allele Identifier: CA368168116

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494491T>A , CM000669.2:g.92494491T>A GRCh38
NC_000007.13:g.92123805T>A , CM000669.1:g.92123805T>A GRCh37
NC_000007.12:g.91961741T>A NCBI36
NG_008341.1:g.39041A>T
NG_008341.2:g.39041A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2922A>T (PEX1) MANE Select ENSP00000248633.4:p.Leu974Phe
ENST00000248633.8:c.2922A>T (PEX1) ENSP00000248633.4:p.Leu974Phe
ENST00000428214.5:c.2751A>T (PEX1) ENSP00000394413.1:p.Leu917Phe
ENST00000438045.5:c.1956A>T (PEX1) ENSP00000410438.1:p.Leu652Phe
ENST00000484913.5:n.2961A>T (PEX1)
ENST00000496420.5:n.2814A>T (PEX1)
NM_000466.2:c.2922A>T (PEX1) NP_000457.1:p.Leu974Phe
NM_001282677.1:c.2751A>T (PEX1) NP_001269606.1:p.Leu917Phe
NM_001282678.1:c.2298A>T (PEX1) NP_001269607.1:p.Leu766Phe
XM_005250433.3:c.1173A>T (PEX1) XP_005250490.1:p.Leu391Phe
XR_242246.3:n.3018A>T (PEX1)
XM_017012319.2:c.1173A>T (PEX1) XP_016867808.1:p.Leu391Phe
XR_001744808.2:n.1949A>T (PEX1)
XR_001744843.2:n.5460T>A (GATAD1)
XR_242246.5:n.2969A>T (PEX1)
XR_927494.3:n.4311T>A (GATAD1)
XR_927503.3:n.4242T>A (GATAD1)
NM_000466.3:c.2922A>T (PEX1) MANE Select NP_000457.1:p.Leu974Phe
NM_001282677.2:c.2751A>T (PEX1) NP_001269606.1:p.Leu917Phe
NM_001282678.2:c.2298A>T (PEX1) NP_001269607.1:p.Leu766Phe