Canonical Allele Identifier: CA421236530
Gene: FLAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154983772G>A , CM000663.2:g.154983772G>A GRCh38
NC_000001.10:g.154956248G>A , CM000663.1:g.154956248G>A GRCh37
NC_000001.9:g.153222872G>A NCBI36
NG_042310.1:g.5479G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292180.8:c.78G>A MANE Select ENSP00000292180.3:p.Lys26=
ENST00000292180.7:c.78G>A ENSP00000292180.3:p.Lys26=
ENST00000315144.14:c.-144-70G>A ENSP00000317296.10:n.-144-70G>A
ENST00000368431.7:c.-789-70G>A ENSP00000357416.3:n.-789-70G>A
ENST00000368432.5:c.-144-70G>A ENSP00000357417.1:n.-144-70G>A
ENST00000368433.5:c.78G>A ENSP00000357418.1:p.Lys26=
ENST00000487371.1:n.204-70G>A
ENST00000492620.1:n.60+375G>A
NM_001184891.1:c.-144-70G>A NP_001171820.1:n.-144-70G>A
NM_001184892.1:c.-789-70G>A NP_001171821.1:n.-789-70G>A
NM_025207.4:c.78G>A NP_079483.3:p.Lys26=
NM_201398.2:c.-144-70G>A NP_958800.1:n.-144-70G>A
XM_005245502.2:c.-144-70G>A XP_005245559.1:n.-144-70G>A
XM_005245503.2:c.-430+375G>A XP_005245560.1:n.-430+375G>A
XM_006711559.2:c.-144-70G>A XP_006711622.1:n.-144-70G>A
XR_241098.3:n.66-70G>A
NM_025207.5:c.78G>A MANE Select NP_079483.3:p.Lys26=
NM_001184891.2:c.-144-70G>A NP_001171820.1:n.-144-70G>A
NM_001184892.2:c.-789-70G>A NP_001171821.1:n.-789-70G>A
NM_201398.3:c.-144-70G>A NP_958800.1:n.-144-70G>A