Canonical Allele Identifier: CA368168433

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494521C>G , CM000669.2:g.92494521C>G GRCh38
NC_000007.13:g.92123835C>G , CM000669.1:g.92123835C>G GRCh37
NC_000007.12:g.91961771C>G NCBI36
NG_008341.1:g.39011G>C
NG_008341.2:g.39011G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2892G>C (PEX1) MANE Select ENSP00000248633.4:p.Leu964Phe
ENST00000248633.8:c.2892G>C (PEX1) ENSP00000248633.4:p.Leu964Phe
ENST00000428214.5:c.2721G>C (PEX1) ENSP00000394413.1:p.Leu907Phe
ENST00000438045.5:c.1926G>C (PEX1) ENSP00000410438.1:p.Leu642Phe
ENST00000484913.5:n.2931G>C (PEX1)
ENST00000496420.5:n.2784G>C (PEX1)
NM_000466.2:c.2892G>C (PEX1) NP_000457.1:p.Leu964Phe
NM_001282677.1:c.2721G>C (PEX1) NP_001269606.1:p.Leu907Phe
NM_001282678.1:c.2268G>C (PEX1) NP_001269607.1:p.Leu756Phe
XM_005250433.3:c.1143G>C (PEX1) XP_005250490.1:p.Leu381Phe
XR_242246.3:n.2988G>C (PEX1)
XM_017012319.2:c.1143G>C (PEX1) XP_016867808.1:p.Leu381Phe
XR_001744808.2:n.1919G>C (PEX1)
XR_001744843.2:n.5490C>G (GATAD1)
XR_242246.5:n.2939G>C (PEX1)
XR_927494.3:n.4341C>G (GATAD1)
XR_927503.3:n.4272C>G (GATAD1)
NM_000466.3:c.2892G>C (PEX1) MANE Select NP_000457.1:p.Leu964Phe
NM_001282677.2:c.2721G>C (PEX1) NP_001269606.1:p.Leu907Phe
NM_001282678.2:c.2268G>C (PEX1) NP_001269607.1:p.Leu756Phe