Canonical Allele Identifier: CA1134397

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988508A>G , CM000663.2:g.154988508A>G	GRCh38
NC_000001.10:g.154960984A>G , CM000663.1:g.154960984A>G	GRCh37
NC_000001.9:g.153227608A>G	NCBI36
NG_042310.1:g.10215A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.776A>G MANE Select	ENSP00000292180.3:p.Glu259Gly
ENST00000292180.7:c.776A>G	ENSP00000292180.3:p.Glu259Gly
ENST00000295530.6:c.-26A>G	ENSP00000295530.2:n.-26A>G
ENST00000315144.14:c.485A>G	ENSP00000317296.10:p.Glu162Gly
ENST00000368431.7:c.479A>G	ENSP00000357416.3:p.Glu160Gly
ENST00000368432.5:c.485A>G	ENSP00000357417.1:p.Glu162Gly
ENST00000368433.5:c.776A>G	ENSP00000357418.1:p.Glu259Gly
NM_001184891.1:c.485A>G	NP_001171820.1:p.Glu162Gly
NM_001184892.1:c.479A>G	NP_001171821.1:p.Glu160Gly
NM_025207.4:c.776A>G	NP_079483.3:p.Glu259Gly
NM_201398.2:c.485A>G	NP_958800.1:p.Glu162Gly
XM_005245502.2:c.485A>G	XP_005245559.1:p.Glu162Gly
XM_005245503.2:c.-26A>G	XP_005245560.1:n.-26A>G
XM_006711559.2:c.485A>G	XP_006711622.1:p.Glu162Gly
XR_241098.3:n.694A>G
NM_025207.5:c.776A>G MANE Select	NP_079483.3:p.Glu259Gly
NM_001184891.2:c.485A>G	NP_001171820.1:p.Glu162Gly
NM_001184892.2:c.479A>G	NP_001171821.1:p.Glu160Gly
NM_201398.3:c.485A>G	NP_958800.1:p.Glu162Gly