Canonical Allele Identifier: CA368168513

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494540T>G , CM000669.2:g.92494540T>G GRCh38
NC_000007.13:g.92123854T>G , CM000669.1:g.92123854T>G GRCh37
NC_000007.12:g.91961790T>G NCBI36
NG_008341.1:g.38992A>C
NG_008341.2:g.38992A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2873A>C (PEX1) MANE Select ENSP00000248633.4:p.Asp958Ala
ENST00000248633.8:c.2873A>C (PEX1) ENSP00000248633.4:p.Asp958Ala
ENST00000428214.5:c.2702A>C (PEX1) ENSP00000394413.1:p.Asp901Ala
ENST00000438045.5:c.1907A>C (PEX1) ENSP00000410438.1:p.Asp636Ala
ENST00000484913.5:n.2912A>C (PEX1)
ENST00000496420.5:n.2765A>C (PEX1)
NM_000466.2:c.2873A>C (PEX1) NP_000457.1:p.Asp958Ala
NM_001282677.1:c.2702A>C (PEX1) NP_001269606.1:p.Asp901Ala
NM_001282678.1:c.2249A>C (PEX1) NP_001269607.1:p.Asp750Ala
XM_005250433.3:c.1124A>C (PEX1) XP_005250490.1:p.Asp375Ala
XR_242246.3:n.2969A>C (PEX1)
XM_017012319.2:c.1124A>C (PEX1) XP_016867808.1:p.Asp375Ala
XR_001744808.2:n.1900A>C (PEX1)
XR_001744843.2:n.5509T>G (GATAD1)
XR_242246.5:n.2920A>C (PEX1)
XR_927494.3:n.4360T>G (GATAD1)
XR_927503.3:n.4291T>G (GATAD1)
NM_000466.3:c.2873A>C (PEX1) MANE Select NP_000457.1:p.Asp958Ala
NM_001282677.2:c.2702A>C (PEX1) NP_001269606.1:p.Asp901Ala
NM_001282678.2:c.2249A>C (PEX1) NP_001269607.1:p.Asp750Ala