Canonical Allele Identifier: CA456624207

Linked Data

MyVariant Identifiers: chr7:g.92120760G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491446G>A , CM000669.2:g.92491446G>A GRCh38
NC_000007.13:g.92120760G>A , CM000669.1:g.92120760G>A GRCh37
NC_000007.12:g.91958696G>A NCBI36
NG_008341.1:g.42086C>T
NG_008341.2:g.42086C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3264C>T (PEX1) MANE Select ENSP00000248633.4:p.Asn1088=
ENST00000248633.8:c.3264C>T (PEX1) ENSP00000248633.4:p.Asn1088=
ENST00000428214.5:c.3093C>T (PEX1) ENSP00000394413.1:p.Asn1031=
ENST00000438045.5:c.2298C>T (PEX1) ENSP00000410438.1:p.Asn766=
ENST00000484913.5:n.3303C>T (PEX1)
ENST00000496420.5:n.4319C>T (PEX1)
NM_000466.2:c.3264C>T (PEX1) NP_000457.1:p.Asn1088=
NM_001282677.1:c.3093C>T (PEX1) NP_001269606.1:p.Asn1031=
NM_001282678.1:c.2640C>T (PEX1) NP_001269607.1:p.Asn880=
XM_005250433.3:c.1515C>T (PEX1) XP_005250490.1:p.Asn505=
XR_242246.3:n.3360C>T (PEX1)
XM_017012319.2:c.1515C>T (PEX1) XP_016867808.1:p.Asn505=
XR_001744808.2:n.2291C>T (PEX1)
XR_001744842.2:n.2484G>A (GATAD1)
XR_001744843.2:n.2415G>A (GATAD1)
XR_002956472.1:n.2541G>A (GATAD1)
XR_002956473.1:n.2572G>A (GATAD1)
XR_002956474.1:n.2489G>A (GATAD1)
XR_242246.5:n.3311C>T (PEX1)
XR_927494.3:n.1266G>A (GATAD1)
XR_927500.3:n.1263G>A (GATAD1)
XR_927503.3:n.1197G>A (GATAD1)
NM_000466.3:c.3264C>T (PEX1) MANE Select NP_000457.1:p.Asn1088=
NM_001282677.2:c.3093C>T (PEX1) NP_001269606.1:p.Asn1031=
NM_001282678.2:c.2640C>T (PEX1) NP_001269607.1:p.Asn880=