Canonical Allele Identifier: CA368164622

Linked Data

gnomAD v4: 7-92491457-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491457C>T , CM000669.2:g.92491457C>T GRCh38
NC_000007.13:g.92120771C>T , CM000669.1:g.92120771C>T GRCh37
NC_000007.12:g.91958707C>T NCBI36
NG_008341.1:g.42075G>A
NG_008341.2:g.42075G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3253G>A (PEX1) MANE Select ENSP00000248633.4:p.Val1085Ile
ENST00000248633.8:c.3253G>A (PEX1) ENSP00000248633.4:p.Val1085Ile
ENST00000428214.5:c.3082G>A (PEX1) ENSP00000394413.1:p.Val1028Ile
ENST00000438045.5:c.2287G>A (PEX1) ENSP00000410438.1:p.Val763Ile
ENST00000484913.5:n.3292G>A (PEX1)
ENST00000496420.5:n.4308G>A (PEX1)
NM_000466.2:c.3253G>A (PEX1) NP_000457.1:p.Val1085Ile
NM_001282677.1:c.3082G>A (PEX1) NP_001269606.1:p.Val1028Ile
NM_001282678.1:c.2629G>A (PEX1) NP_001269607.1:p.Val877Ile
XM_005250433.3:c.1504G>A (PEX1) XP_005250490.1:p.Val502Ile
XR_242246.3:n.3349G>A (PEX1)
XM_017012319.2:c.1504G>A (PEX1) XP_016867808.1:p.Val502Ile
XR_001744808.2:n.2280G>A (PEX1)
XR_001744842.2:n.2495C>T (GATAD1)
XR_001744843.2:n.2426C>T (GATAD1)
XR_002956472.1:n.2552C>T (GATAD1)
XR_002956473.1:n.2583C>T (GATAD1)
XR_002956474.1:n.2500C>T (GATAD1)
XR_242246.5:n.3300G>A (PEX1)
XR_927494.3:n.1277C>T (GATAD1)
XR_927500.3:n.1274C>T (GATAD1)
XR_927503.3:n.1208C>T (GATAD1)
NM_000466.3:c.3253G>A (PEX1) MANE Select NP_000457.1:p.Val1085Ile
NM_001282677.2:c.3082G>A (PEX1) NP_001269606.1:p.Val1028Ile
NM_001282678.2:c.2629G>A (PEX1) NP_001269607.1:p.Val877Ile