Canonical Allele Identifier: CA368167864

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494390T>C , CM000669.2:g.92494390T>C GRCh38
NC_000007.13:g.92123704T>C , CM000669.1:g.92123704T>C GRCh37
NC_000007.12:g.91961640T>C NCBI36
NG_008341.1:g.39142A>G
NG_008341.2:g.39142A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2933A>G (PEX1) MANE Select ENSP00000248633.4:p.Tyr978Cys
ENST00000248633.8:c.2933A>G (PEX1) ENSP00000248633.4:p.Tyr978Cys
ENST00000428214.5:c.2762A>G (PEX1) ENSP00000394413.1:p.Tyr921Cys
ENST00000438045.5:c.1967A>G (PEX1) ENSP00000410438.1:p.Tyr656Cys
ENST00000484913.5:n.2972A>G (PEX1)
ENST00000496420.5:n.2825A>G (PEX1)
NM_000466.2:c.2933A>G (PEX1) NP_000457.1:p.Tyr978Cys
NM_001282677.1:c.2762A>G (PEX1) NP_001269606.1:p.Tyr921Cys
NM_001282678.1:c.2309A>G (PEX1) NP_001269607.1:p.Tyr770Cys
XM_005250433.3:c.1184A>G (PEX1) XP_005250490.1:p.Tyr395Cys
XR_242246.3:n.3029A>G (PEX1)
XM_017012319.2:c.1184A>G (PEX1) XP_016867808.1:p.Tyr395Cys
XR_001744808.2:n.1960A>G (PEX1)
XR_001744843.2:n.5359T>C (GATAD1)
XR_242246.5:n.2980A>G (PEX1)
XR_927494.3:n.4210T>C (GATAD1)
XR_927503.3:n.4141T>C (GATAD1)
NM_000466.3:c.2933A>G (PEX1) MANE Select NP_000457.1:p.Tyr978Cys
NM_001282677.2:c.2762A>G (PEX1) NP_001269606.1:p.Tyr921Cys
NM_001282678.2:c.2309A>G (PEX1) NP_001269607.1:p.Tyr770Cys