Canonical Allele Identifier: CA368168456

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494525T>G , CM000669.2:g.92494525T>G GRCh38
NC_000007.13:g.92123839T>G , CM000669.1:g.92123839T>G GRCh37
NC_000007.12:g.91961775T>G NCBI36
NG_008341.1:g.39007A>C
NG_008341.2:g.39007A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2888A>C (PEX1) MANE Select ENSP00000248633.4:p.Gln963Pro
ENST00000248633.8:c.2888A>C (PEX1) ENSP00000248633.4:p.Gln963Pro
ENST00000428214.5:c.2717A>C (PEX1) ENSP00000394413.1:p.Gln906Pro
ENST00000438045.5:c.1922A>C (PEX1) ENSP00000410438.1:p.Gln641Pro
ENST00000484913.5:n.2927A>C (PEX1)
ENST00000496420.5:n.2780A>C (PEX1)
NM_000466.2:c.2888A>C (PEX1) NP_000457.1:p.Gln963Pro
NM_001282677.1:c.2717A>C (PEX1) NP_001269606.1:p.Gln906Pro
NM_001282678.1:c.2264A>C (PEX1) NP_001269607.1:p.Gln755Pro
XM_005250433.3:c.1139A>C (PEX1) XP_005250490.1:p.Gln380Pro
XR_242246.3:n.2984A>C (PEX1)
XM_017012319.2:c.1139A>C (PEX1) XP_016867808.1:p.Gln380Pro
XR_001744808.2:n.1915A>C (PEX1)
XR_001744843.2:n.5494T>G (GATAD1)
XR_242246.5:n.2935A>C (PEX1)
XR_927494.3:n.4345T>G (GATAD1)
XR_927503.3:n.4276T>G (GATAD1)
NM_000466.3:c.2888A>C (PEX1) MANE Select NP_000457.1:p.Gln963Pro
NM_001282677.2:c.2717A>C (PEX1) NP_001269606.1:p.Gln906Pro
NM_001282678.2:c.2264A>C (PEX1) NP_001269607.1:p.Gln755Pro