Canonical Allele Identifier: CA456624336

Linked Data

MyVariant Identifiers: chr7:g.92120793A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491479A>G , CM000669.2:g.92491479A>G GRCh38
NC_000007.13:g.92120793A>G , CM000669.1:g.92120793A>G GRCh37
NC_000007.12:g.91958729A>G NCBI36
NG_008341.1:g.42053T>C
NG_008341.2:g.42053T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3231T>C (PEX1) MANE Select ENSP00000248633.4:p.Ser1077=
ENST00000248633.8:c.3231T>C (PEX1) ENSP00000248633.4:p.Ser1077=
ENST00000428214.5:c.3060T>C (PEX1) ENSP00000394413.1:p.Ser1020=
ENST00000438045.5:c.2265T>C (PEX1) ENSP00000410438.1:p.Ser755=
ENST00000484913.5:n.3270T>C (PEX1)
ENST00000496420.5:n.4286T>C (PEX1)
NM_000466.2:c.3231T>C (PEX1) NP_000457.1:p.Ser1077=
NM_001282677.1:c.3060T>C (PEX1) NP_001269606.1:p.Ser1020=
NM_001282678.1:c.2607T>C (PEX1) NP_001269607.1:p.Ser869=
XM_005250433.3:c.1482T>C (PEX1) XP_005250490.1:p.Ser494=
XR_242246.3:n.3327T>C (PEX1)
XM_017012319.2:c.1482T>C (PEX1) XP_016867808.1:p.Ser494=
XR_001744808.2:n.2258T>C (PEX1)
XR_001744842.2:n.2517A>G (GATAD1)
XR_001744843.2:n.2448A>G (GATAD1)
XR_002956472.1:n.2574A>G (GATAD1)
XR_002956473.1:n.2605A>G (GATAD1)
XR_002956474.1:n.2522A>G (GATAD1)
XR_242246.5:n.3278T>C (PEX1)
XR_927494.3:n.1299A>G (GATAD1)
XR_927500.3:n.1296A>G (GATAD1)
XR_927503.3:n.1230A>G (GATAD1)
NM_000466.3:c.3231T>C (PEX1) MANE Select NP_000457.1:p.Ser1077=
NM_001282677.2:c.3060T>C (PEX1) NP_001269606.1:p.Ser1020=
NM_001282678.2:c.2607T>C (PEX1) NP_001269607.1:p.Ser869=