Canonical Allele Identifier: CA368164420

Linked Data

gnomAD v4: 7-92491435-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491435C>T , CM000669.2:g.92491435C>T GRCh38
NC_000007.13:g.92120749C>T , CM000669.1:g.92120749C>T GRCh37
NC_000007.12:g.91958685C>T NCBI36
NG_008341.1:g.42097G>A
NG_008341.2:g.42097G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3275G>A (PEX1) MANE Select ENSP00000248633.4:p.Gly1092Asp
ENST00000248633.8:c.3275G>A (PEX1) ENSP00000248633.4:p.Gly1092Asp
ENST00000428214.5:c.3104G>A (PEX1) ENSP00000394413.1:p.Gly1035Asp
ENST00000438045.5:c.2309G>A (PEX1) ENSP00000410438.1:p.Gly770Asp
ENST00000484913.5:n.3314G>A (PEX1)
ENST00000496420.5:n.4330G>A (PEX1)
NM_000466.2:c.3275G>A (PEX1) NP_000457.1:p.Gly1092Asp
NM_001282677.1:c.3104G>A (PEX1) NP_001269606.1:p.Gly1035Asp
NM_001282678.1:c.2651G>A (PEX1) NP_001269607.1:p.Gly884Asp
XM_005250433.3:c.1526G>A (PEX1) XP_005250490.1:p.Gly509Asp
XR_242246.3:n.3371G>A (PEX1)
XM_017012319.2:c.1526G>A (PEX1) XP_016867808.1:p.Gly509Asp
XR_001744808.2:n.2302G>A (PEX1)
XR_001744842.2:n.2473C>T (GATAD1)
XR_001744843.2:n.2404C>T (GATAD1)
XR_002956472.1:n.2530C>T (GATAD1)
XR_002956473.1:n.2561C>T (GATAD1)
XR_002956474.1:n.2478C>T (GATAD1)
XR_242246.5:n.3322G>A (PEX1)
XR_927494.3:n.1255C>T (GATAD1)
XR_927500.3:n.1252C>T (GATAD1)
XR_927503.3:n.1186C>T (GATAD1)
NM_000466.3:c.3275G>A (PEX1) MANE Select NP_000457.1:p.Gly1092Asp
NM_001282677.2:c.3104G>A (PEX1) NP_001269606.1:p.Gly1035Asp
NM_001282678.2:c.2651G>A (PEX1) NP_001269607.1:p.Gly884Asp