Canonical Allele Identifier: CA368161535

Linked Data

gnomAD v4: 7-92489799-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489799C>A , CM000669.2:g.92489799C>A GRCh38
NC_000007.13:g.92119113C>A , CM000669.1:g.92119113C>A GRCh37
NC_000007.12:g.91957049C>A NCBI36
NG_008341.1:g.43733G>T
NG_008341.2:g.43733G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3551G>T (PEX1) MANE Select ENSP00000248633.4:p.Gly1184Val
ENST00000248633.8:c.3551G>T (PEX1) ENSP00000248633.4:p.Gly1184Val
ENST00000428214.5:c.3380G>T (PEX1) ENSP00000394413.1:p.Gly1127Val
ENST00000438045.5:c.2585G>T (PEX1) ENSP00000410438.1:p.Gly862Val
ENST00000469417.1:n.448G>T (PEX1)
ENST00000484913.5:n.3590G>T (PEX1)
ENST00000496420.5:n.4606G>T (PEX1)
NM_000466.2:c.3551G>T (PEX1) NP_000457.1:p.Gly1184Val
NM_001282677.1:c.3380G>T (PEX1) NP_001269606.1:p.Gly1127Val
NM_001282678.1:c.2927G>T (PEX1) NP_001269607.1:p.Gly976Val
XM_005250433.3:c.1802G>T (PEX1) XP_005250490.1:p.Gly601Val
XR_242246.3:n.3647G>T (PEX1)
XR_927494.1:n.1036-1444C>A (GATAD1)
XR_927495.1:n.1036-287C>A (GATAD1)
XR_927496.1:n.1041-1444C>A (GATAD1)
XR_927497.1:n.1036-287C>A (GATAD1)
XR_927498.1:n.1124-1444C>A (GATAD1)
XR_927500.1:n.1033-1444C>A (GATAD1)
XR_927502.1:n.1033-287C>A (GATAD1)
XR_927503.1:n.967-1444C>A (GATAD1)
XM_017012319.2:c.1802G>T (PEX1) XP_016867808.1:p.Gly601Val
XR_001744808.2:n.2578G>T (PEX1)
XR_001744842.2:n.2281-1444C>A (GATAD1)
XR_001744843.2:n.2212-1444C>A (GATAD1)
XR_002956472.1:n.2281-287C>A (GATAD1)
XR_002956473.1:n.2369-1444C>A (GATAD1)
XR_002956474.1:n.2286-1444C>A (GATAD1)
XR_242246.5:n.3598G>T (PEX1)
XR_927494.3:n.1063-1444C>A (GATAD1)
XR_927500.3:n.1060-1444C>A (GATAD1)
XR_927503.3:n.994-1444C>A (GATAD1)
NM_000466.3:c.3551G>T (PEX1) MANE Select NP_000457.1:p.Gly1184Val
NM_001282677.2:c.3380G>T (PEX1) NP_001269606.1:p.Gly1127Val
NM_001282678.2:c.2927G>T (PEX1) NP_001269607.1:p.Gly976Val