Canonical Allele Identifier: CA368167725

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494375G>A , CM000669.2:g.92494375G>A GRCh38
NC_000007.13:g.92123689G>A , CM000669.1:g.92123689G>A GRCh37
NC_000007.12:g.91961625G>A NCBI36
NG_008341.1:g.39157C>T
NG_008341.2:g.39157C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2948C>T (PEX1) MANE Select ENSP00000248633.4:p.Thr983Ile
ENST00000248633.8:c.2948C>T (PEX1) ENSP00000248633.4:p.Thr983Ile
ENST00000428214.5:c.2777C>T (PEX1) ENSP00000394413.1:p.Thr926Ile
ENST00000438045.5:c.1982C>T (PEX1) ENSP00000410438.1:p.Thr661Ile
ENST00000484913.5:n.2987C>T (PEX1)
ENST00000496420.5:n.2840C>T (PEX1)
NM_000466.2:c.2948C>T (PEX1) NP_000457.1:p.Thr983Ile
NM_001282677.1:c.2777C>T (PEX1) NP_001269606.1:p.Thr926Ile
NM_001282678.1:c.2324C>T (PEX1) NP_001269607.1:p.Thr775Ile
XM_005250433.3:c.1199C>T (PEX1) XP_005250490.1:p.Thr400Ile
XR_242246.3:n.3044C>T (PEX1)
XM_017012319.2:c.1199C>T (PEX1) XP_016867808.1:p.Thr400Ile
XR_001744808.2:n.1975C>T (PEX1)
XR_001744843.2:n.5344G>A (GATAD1)
XR_242246.5:n.2995C>T (PEX1)
XR_927494.3:n.4195G>A (GATAD1)
XR_927503.3:n.4126G>A (GATAD1)
NM_000466.3:c.2948C>T (PEX1) MANE Select NP_000457.1:p.Thr983Ile
NM_001282677.2:c.2777C>T (PEX1) NP_001269606.1:p.Thr926Ile
NM_001282678.2:c.2324C>T (PEX1) NP_001269607.1:p.Thr775Ile