Canonical Allele Identifier: CA1134366

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988380C>A , CM000663.2:g.154988380C>A	GRCh38
NC_000001.10:g.154960856C>A , CM000663.1:g.154960856C>A	GRCh37
NC_000001.9:g.153227480C>A	NCBI36
NG_042310.1:g.10087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.648C>A MANE Select	ENSP00000292180.3:p.Gly216=
ENST00000292180.7:c.648C>A	ENSP00000292180.3:p.Gly216=
ENST00000295530.6:c.-154C>A	ENSP00000295530.2:n.-154C>A
ENST00000315144.14:c.357C>A	ENSP00000317296.10:p.Gly119=
ENST00000368431.7:c.351C>A	ENSP00000357416.3:p.Gly117=
ENST00000368432.5:c.357C>A	ENSP00000357417.1:p.Gly119=
ENST00000368433.5:c.648C>A	ENSP00000357418.1:p.Gly216=
ENST00000487371.1:n.704C>A
NM_001184891.1:c.357C>A	NP_001171820.1:p.Gly119=
NM_001184892.1:c.351C>A	NP_001171821.1:p.Gly117=
NM_025207.4:c.648C>A	NP_079483.3:p.Gly216=
NM_201398.2:c.357C>A	NP_958800.1:p.Gly119=
XM_005245502.2:c.357C>A	XP_005245559.1:p.Gly119=
XM_005245503.2:c.-154C>A	XP_005245560.1:n.-154C>A
XM_006711559.2:c.357C>A	XP_006711622.1:p.Gly119=
XR_241098.3:n.566C>A
NM_025207.5:c.648C>A MANE Select	NP_079483.3:p.Gly216=
NM_001184891.2:c.357C>A	NP_001171820.1:p.Gly119=
NM_001184892.2:c.351C>A	NP_001171821.1:p.Gly117=
NM_201398.3:c.357C>A	NP_958800.1:p.Gly119=