Canonical Allele Identifier: CA2481096896
Gene: FLAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154988051C= , CM000663.2:g.154988051C= GRCh38
NC_000001.10:g.154960527C= , CM000663.1:g.154960527C= GRCh37
NC_000001.9:g.153227151C= NCBI36
NG_042310.1:g.9758C=

Transcript Alleles

HGVS Amino-acid change
ENST00000292180.8:c.373-54C= MANE Select ENSP00000292180.3:n.373-54C=
ENST00000292180.7:c.373-54C= ENSP00000292180.3:n.373-54C=
ENST00000315144.14:c.82-54C= ENSP00000317296.10:n.82-54C=
ENST00000368431.7:c.22C= ENSP00000357416.3:p.Pro8=
ENST00000368432.5:c.82-54C= ENSP00000357417.1:n.82-54C=
ENST00000368433.5:c.373-54C= ENSP00000357418.1:n.373-54C=
ENST00000487371.1:n.429-54C=
ENST00000492620.1:n.646C=
NM_001184891.1:c.82-54C= NP_001171820.1:n.82-54C=
NM_001184892.1:c.22C= NP_001171821.1:p.Pro8=
NM_025207.4:c.373-54C= NP_079483.3:n.373-54C=
NM_201398.2:c.82-54C= NP_958800.1:n.82-54C=
XM_005245502.2:c.82-54C= XP_005245559.1:n.82-54C=
XM_005245503.2:c.-429-54C= XP_005245560.1:n.-429-54C=
XM_006711559.2:c.82-54C= XP_006711622.1:n.82-54C=
XR_241098.3:n.291-54C=
NM_025207.5:c.373-54C= MANE Select NP_079483.3:n.373-54C=
NM_001184891.2:c.82-54C= NP_001171820.1:n.82-54C=
NM_001184892.2:c.22C= NP_001171821.1:p.Pro8=
NM_201398.3:c.82-54C= NP_958800.1:n.82-54C=