Canonical Allele Identifier: CA456480730

Linked Data

MyVariant Identifiers: chr7:g.92119132T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489818T>G , CM000669.2:g.92489818T>G GRCh38
NC_000007.13:g.92119132T>G , CM000669.1:g.92119132T>G GRCh37
NC_000007.12:g.91957068T>G NCBI36
NG_008341.1:g.43714A>C
NG_008341.2:g.43714A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3532A>C (PEX1) MANE Select ENSP00000248633.4:p.Arg1178=
ENST00000248633.8:c.3532A>C (PEX1) ENSP00000248633.4:p.Arg1178=
ENST00000428214.5:c.3361A>C (PEX1) ENSP00000394413.1:p.Arg1121=
ENST00000438045.5:c.2566A>C (PEX1) ENSP00000410438.1:p.Arg856=
ENST00000469417.1:n.429A>C (PEX1)
ENST00000484913.5:n.3571A>C (PEX1)
ENST00000496420.5:n.4587A>C (PEX1)
NM_000466.2:c.3532A>C (PEX1) NP_000457.1:p.Arg1178=
NM_001282677.1:c.3361A>C (PEX1) NP_001269606.1:p.Arg1121=
NM_001282678.1:c.2908A>C (PEX1) NP_001269607.1:p.Arg970=
XM_005250433.3:c.1783A>C (PEX1) XP_005250490.1:p.Arg595=
XR_242246.3:n.3628A>C (PEX1)
XR_927494.1:n.1036-1425T>G (GATAD1)
XR_927495.1:n.1036-268T>G (GATAD1)
XR_927496.1:n.1041-1425T>G (GATAD1)
XR_927497.1:n.1036-268T>G (GATAD1)
XR_927498.1:n.1124-1425T>G (GATAD1)
XR_927500.1:n.1033-1425T>G (GATAD1)
XR_927502.1:n.1033-268T>G (GATAD1)
XR_927503.1:n.967-1425T>G (GATAD1)
XM_017012319.2:c.1783A>C (PEX1) XP_016867808.1:p.Arg595=
XR_001744808.2:n.2559A>C (PEX1)
XR_001744842.2:n.2281-1425T>G (GATAD1)
XR_001744843.2:n.2212-1425T>G (GATAD1)
XR_002956472.1:n.2281-268T>G (GATAD1)
XR_002956473.1:n.2369-1425T>G (GATAD1)
XR_002956474.1:n.2286-1425T>G (GATAD1)
XR_242246.5:n.3579A>C (PEX1)
XR_927494.3:n.1063-1425T>G (GATAD1)
XR_927500.3:n.1060-1425T>G (GATAD1)
XR_927503.3:n.994-1425T>G (GATAD1)
NM_000466.3:c.3532A>C (PEX1) MANE Select NP_000457.1:p.Arg1178=
NM_001282677.2:c.3361A>C (PEX1) NP_001269606.1:p.Arg1121=
NM_001282678.2:c.2908A>C (PEX1) NP_001269607.1:p.Arg970=