Canonical Allele Identifier: CA456480591

Linked Data

gnomAD v4: 7-92489786-A-G
MyVariant Identifiers: chr7:g.92119100A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489786A>G , CM000669.2:g.92489786A>G GRCh38
NC_000007.13:g.92119100A>G , CM000669.1:g.92119100A>G GRCh37
NC_000007.12:g.91957036A>G NCBI36
NG_008341.1:g.43746T>C
NG_008341.2:g.43746T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3564T>C (PEX1) MANE Select ENSP00000248633.4:p.Leu1188=
ENST00000248633.8:c.3564T>C (PEX1) ENSP00000248633.4:p.Leu1188=
ENST00000428214.5:c.3393T>C (PEX1) ENSP00000394413.1:p.Leu1131=
ENST00000438045.5:c.2598T>C (PEX1) ENSP00000410438.1:p.Leu866=
ENST00000469417.1:n.461T>C (PEX1)
ENST00000477342.1:n.9T>C (PEX1)
ENST00000484913.5:n.3603T>C (PEX1)
ENST00000496420.5:n.4619T>C (PEX1)
NM_000466.2:c.3564T>C (PEX1) NP_000457.1:p.Leu1188=
NM_001282677.1:c.3393T>C (PEX1) NP_001269606.1:p.Leu1131=
NM_001282678.1:c.2940T>C (PEX1) NP_001269607.1:p.Leu980=
XM_005250433.3:c.1815T>C (PEX1) XP_005250490.1:p.Leu605=
XR_242246.3:n.3660T>C (PEX1)
XR_927494.1:n.1036-1457A>G (GATAD1)
XR_927495.1:n.1036-300A>G (GATAD1)
XR_927496.1:n.1041-1457A>G (GATAD1)
XR_927497.1:n.1036-300A>G (GATAD1)
XR_927498.1:n.1124-1457A>G (GATAD1)
XR_927500.1:n.1033-1457A>G (GATAD1)
XR_927502.1:n.1033-300A>G (GATAD1)
XR_927503.1:n.967-1457A>G (GATAD1)
XM_017012319.2:c.1815T>C (PEX1) XP_016867808.1:p.Leu605=
XR_001744808.2:n.2591T>C (PEX1)
XR_001744842.2:n.2281-1457A>G (GATAD1)
XR_001744843.2:n.2212-1457A>G (GATAD1)
XR_002956472.1:n.2281-300A>G (GATAD1)
XR_002956473.1:n.2369-1457A>G (GATAD1)
XR_002956474.1:n.2286-1457A>G (GATAD1)
XR_242246.5:n.3611T>C (PEX1)
XR_927494.3:n.1063-1457A>G (GATAD1)
XR_927500.3:n.1060-1457A>G (GATAD1)
XR_927503.3:n.994-1457A>G (GATAD1)
NM_000466.3:c.3564T>C (PEX1) MANE Select NP_000457.1:p.Leu1188=
NM_001282677.2:c.3393T>C (PEX1) NP_001269606.1:p.Leu1131=
NM_001282678.2:c.2940T>C (PEX1) NP_001269607.1:p.Leu980=