Canonical Allele Identifier: CA456624408

Linked Data

MyVariant Identifiers: chr7:g.92120811T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491497T>A , CM000669.2:g.92491497T>A GRCh38
NC_000007.13:g.92120811T>A , CM000669.1:g.92120811T>A GRCh37
NC_000007.12:g.91958747T>A NCBI36
NG_008341.1:g.42035A>T
NG_008341.2:g.42035A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3213A>T (PEX1) MANE Select ENSP00000248633.4:p.Gly1071=
ENST00000248633.8:c.3213A>T (PEX1) ENSP00000248633.4:p.Gly1071=
ENST00000428214.5:c.3042A>T (PEX1) ENSP00000394413.1:p.Gly1014=
ENST00000438045.5:c.2247A>T (PEX1) ENSP00000410438.1:p.Gly749=
ENST00000484913.5:n.3252A>T (PEX1)
ENST00000496420.5:n.4268A>T (PEX1)
NM_000466.2:c.3213A>T (PEX1) NP_000457.1:p.Gly1071=
NM_001282677.1:c.3042A>T (PEX1) NP_001269606.1:p.Gly1014=
NM_001282678.1:c.2589A>T (PEX1) NP_001269607.1:p.Gly863=
XM_005250433.3:c.1464A>T (PEX1) XP_005250490.1:p.Gly488=
XR_242246.3:n.3309A>T (PEX1)
XM_017012319.2:c.1464A>T (PEX1) XP_016867808.1:p.Gly488=
XR_001744808.2:n.2240A>T (PEX1)
XR_001744842.2:n.2535T>A (GATAD1)
XR_001744843.2:n.2466T>A (GATAD1)
XR_002956472.1:n.2592T>A (GATAD1)
XR_002956473.1:n.2623T>A (GATAD1)
XR_002956474.1:n.2540T>A (GATAD1)
XR_242246.5:n.3260A>T (PEX1)
XR_927494.3:n.1317T>A (GATAD1)
XR_927500.3:n.1314T>A (GATAD1)
XR_927503.3:n.1248T>A (GATAD1)
NM_000466.3:c.3213A>T (PEX1) MANE Select NP_000457.1:p.Gly1071=
NM_001282677.2:c.3042A>T (PEX1) NP_001269606.1:p.Gly1014=
NM_001282678.2:c.2589A>T (PEX1) NP_001269607.1:p.Gly863=