Canonical Allele Identifier: CA368167262

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494294T>G , CM000669.2:g.92494294T>G GRCh38
NC_000007.13:g.92123608T>G , CM000669.1:g.92123608T>G GRCh37
NC_000007.12:g.91961544T>G NCBI36
NG_008341.1:g.39238A>C
NG_008341.2:g.39238A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3029A>C (PEX1) MANE Select ENSP00000248633.4:p.Gln1010Pro
ENST00000248633.8:c.3029A>C (PEX1) ENSP00000248633.4:p.Gln1010Pro
ENST00000428214.5:c.2858A>C (PEX1) ENSP00000394413.1:p.Gln953Pro
ENST00000438045.5:c.2063A>C (PEX1) ENSP00000410438.1:p.Gln688Pro
ENST00000484913.5:n.3068A>C (PEX1)
ENST00000496420.5:n.2921A>C (PEX1)
NM_000466.2:c.3029A>C (PEX1) NP_000457.1:p.Gln1010Pro
NM_001282677.1:c.2858A>C (PEX1) NP_001269606.1:p.Gln953Pro
NM_001282678.1:c.2405A>C (PEX1) NP_001269607.1:p.Gln802Pro
XM_005250433.3:c.1280A>C (PEX1) XP_005250490.1:p.Gln427Pro
XR_242246.3:n.3125A>C (PEX1)
XM_017012319.2:c.1280A>C (PEX1) XP_016867808.1:p.Gln427Pro
XR_001744808.2:n.2056A>C (PEX1)
XR_001744843.2:n.5263T>G (GATAD1)
XR_242246.5:n.3076A>C (PEX1)
XR_927494.3:n.4114T>G (GATAD1)
XR_927503.3:n.4045T>G (GATAD1)
NM_000466.3:c.3029A>C (PEX1) MANE Select NP_000457.1:p.Gln1010Pro
NM_001282677.2:c.2858A>C (PEX1) NP_001269606.1:p.Gln953Pro
NM_001282678.2:c.2405A>C (PEX1) NP_001269607.1:p.Gln802Pro