Canonical Allele Identifier: CA456480615

Linked Data

MyVariant Identifiers: chr7:g.92119106T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489792T>C , CM000669.2:g.92489792T>C GRCh38
NC_000007.13:g.92119106T>C , CM000669.1:g.92119106T>C GRCh37
NC_000007.12:g.91957042T>C NCBI36
NG_008341.1:g.43740A>G
NG_008341.2:g.43740A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3558A>G (PEX1) MANE Select ENSP00000248633.4:p.Gln1186=
ENST00000248633.8:c.3558A>G (PEX1) ENSP00000248633.4:p.Gln1186=
ENST00000428214.5:c.3387A>G (PEX1) ENSP00000394413.1:p.Gln1129=
ENST00000438045.5:c.2592A>G (PEX1) ENSP00000410438.1:p.Gln864=
ENST00000469417.1:n.455A>G (PEX1)
ENST00000477342.1:n.3A>G (PEX1)
ENST00000484913.5:n.3597A>G (PEX1)
ENST00000496420.5:n.4613A>G (PEX1)
NM_000466.2:c.3558A>G (PEX1) NP_000457.1:p.Gln1186=
NM_001282677.1:c.3387A>G (PEX1) NP_001269606.1:p.Gln1129=
NM_001282678.1:c.2934A>G (PEX1) NP_001269607.1:p.Gln978=
XM_005250433.3:c.1809A>G (PEX1) XP_005250490.1:p.Gln603=
XR_242246.3:n.3654A>G (PEX1)
XR_927494.1:n.1036-1451T>C (GATAD1)
XR_927495.1:n.1036-294T>C (GATAD1)
XR_927496.1:n.1041-1451T>C (GATAD1)
XR_927497.1:n.1036-294T>C (GATAD1)
XR_927498.1:n.1124-1451T>C (GATAD1)
XR_927500.1:n.1033-1451T>C (GATAD1)
XR_927502.1:n.1033-294T>C (GATAD1)
XR_927503.1:n.967-1451T>C (GATAD1)
XM_017012319.2:c.1809A>G (PEX1) XP_016867808.1:p.Gln603=
XR_001744808.2:n.2585A>G (PEX1)
XR_001744842.2:n.2281-1451T>C (GATAD1)
XR_001744843.2:n.2212-1451T>C (GATAD1)
XR_002956472.1:n.2281-294T>C (GATAD1)
XR_002956473.1:n.2369-1451T>C (GATAD1)
XR_002956474.1:n.2286-1451T>C (GATAD1)
XR_242246.5:n.3605A>G (PEX1)
XR_927494.3:n.1063-1451T>C (GATAD1)
XR_927500.3:n.1060-1451T>C (GATAD1)
XR_927503.3:n.994-1451T>C (GATAD1)
NM_000466.3:c.3558A>G (PEX1) MANE Select NP_000457.1:p.Gln1186=
NM_001282677.2:c.3387A>G (PEX1) NP_001269606.1:p.Gln1129=
NM_001282678.2:c.2934A>G (PEX1) NP_001269607.1:p.Gln978=