Canonical Allele Identifier: CA1134361
Gene: FLAD1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154988359C>T , CM000663.2:g.154988359C>T GRCh38
NC_000001.10:g.154960835C>T , CM000663.1:g.154960835C>T GRCh37
NC_000001.9:g.153227459C>T NCBI36
NG_042310.1:g.10066C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292180.8:c.627C>T MANE Select ENSP00000292180.3:p.Thr209=
ENST00000292180.7:c.627C>T ENSP00000292180.3:p.Thr209=
ENST00000295530.6:c.-175C>T ENSP00000295530.2:n.-175C>T
ENST00000315144.14:c.336C>T ENSP00000317296.10:p.Thr112=
ENST00000368431.7:c.330C>T ENSP00000357416.3:p.Thr110=
ENST00000368432.5:c.336C>T ENSP00000357417.1:p.Thr112=
ENST00000368433.5:c.627C>T ENSP00000357418.1:p.Thr209=
ENST00000487371.1:n.683C>T
NM_001184891.1:c.336C>T NP_001171820.1:p.Thr112=
NM_001184892.1:c.330C>T NP_001171821.1:p.Thr110=
NM_025207.4:c.627C>T NP_079483.3:p.Thr209=
NM_201398.2:c.336C>T NP_958800.1:p.Thr112=
XM_005245502.2:c.336C>T XP_005245559.1:p.Thr112=
XM_005245503.2:c.-175C>T XP_005245560.1:n.-175C>T
XM_006711559.2:c.336C>T XP_006711622.1:p.Thr112=
XR_241098.3:n.545C>T
NM_025207.5:c.627C>T MANE Select NP_079483.3:p.Thr209=
NM_001184891.2:c.336C>T NP_001171820.1:p.Thr112=
NM_001184892.2:c.330C>T NP_001171821.1:p.Thr110=
NM_201398.3:c.336C>T NP_958800.1:p.Thr112=