Canonical Allele Identifier: CA1134331

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988173C>T , CM000663.2:g.154988173C>T	GRCh38
NC_000001.10:g.154960649C>T , CM000663.1:g.154960649C>T	GRCh37
NC_000001.9:g.153227273C>T	NCBI36
NG_042310.1:g.9880C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.441C>T MANE Select	ENSP00000292180.3:p.Cys147=
ENST00000292180.7:c.441C>T	ENSP00000292180.3:p.Cys147=
ENST00000295530.6:c.-361C>T	ENSP00000295530.2:n.-361C>T
ENST00000315144.14:c.150C>T	ENSP00000317296.10:p.Cys50=
ENST00000368431.7:c.144C>T	ENSP00000357416.3:p.Cys48=
ENST00000368432.5:c.150C>T	ENSP00000357417.1:p.Cys50=
ENST00000368433.5:c.441C>T	ENSP00000357418.1:p.Cys147=
ENST00000487371.1:n.497C>T
NM_001184891.1:c.150C>T	NP_001171820.1:p.Cys50=
NM_001184892.1:c.144C>T	NP_001171821.1:p.Cys48=
NM_025207.4:c.441C>T	NP_079483.3:p.Cys147=
NM_201398.2:c.150C>T	NP_958800.1:p.Cys50=
XM_005245502.2:c.150C>T	XP_005245559.1:p.Cys50=
XM_005245503.2:c.-361C>T	XP_005245560.1:n.-361C>T
XM_006711559.2:c.150C>T	XP_006711622.1:p.Cys50=
XR_241098.3:n.359C>T
NM_025207.5:c.441C>T MANE Select	NP_079483.3:p.Cys147=
NM_001184891.2:c.150C>T	NP_001171820.1:p.Cys50=
NM_001184892.2:c.144C>T	NP_001171821.1:p.Cys48=
NM_201398.3:c.150C>T	NP_958800.1:p.Cys50=