Canonical Allele Identifier: CA368168459

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494526G>T , CM000669.2:g.92494526G>T GRCh38
NC_000007.13:g.92123840G>T , CM000669.1:g.92123840G>T GRCh37
NC_000007.12:g.91961776G>T NCBI36
NG_008341.1:g.39006C>A
NG_008341.2:g.39006C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2887C>A (PEX1) MANE Select ENSP00000248633.4:p.Gln963Lys
ENST00000248633.8:c.2887C>A (PEX1) ENSP00000248633.4:p.Gln963Lys
ENST00000428214.5:c.2716C>A (PEX1) ENSP00000394413.1:p.Gln906Lys
ENST00000438045.5:c.1921C>A (PEX1) ENSP00000410438.1:p.Gln641Lys
ENST00000484913.5:n.2926C>A (PEX1)
ENST00000496420.5:n.2779C>A (PEX1)
NM_000466.2:c.2887C>A (PEX1) NP_000457.1:p.Gln963Lys
NM_001282677.1:c.2716C>A (PEX1) NP_001269606.1:p.Gln906Lys
NM_001282678.1:c.2263C>A (PEX1) NP_001269607.1:p.Gln755Lys
XM_005250433.3:c.1138C>A (PEX1) XP_005250490.1:p.Gln380Lys
XR_242246.3:n.2983C>A (PEX1)
XM_017012319.2:c.1138C>A (PEX1) XP_016867808.1:p.Gln380Lys
XR_001744808.2:n.1914C>A (PEX1)
XR_001744843.2:n.5495G>T (GATAD1)
XR_242246.5:n.2934C>A (PEX1)
XR_927494.3:n.4346G>T (GATAD1)
XR_927503.3:n.4277G>T (GATAD1)
NM_000466.3:c.2887C>A (PEX1) MANE Select NP_000457.1:p.Gln963Lys
NM_001282677.2:c.2716C>A (PEX1) NP_001269606.1:p.Gln906Lys
NM_001282678.2:c.2263C>A (PEX1) NP_001269607.1:p.Gln755Lys