Canonical Allele Identifier: CA1134370

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988414C>T , CM000663.2:g.154988414C>T	GRCh38
NC_000001.10:g.154960890C>T , CM000663.1:g.154960890C>T	GRCh37
NC_000001.9:g.153227514C>T	NCBI36
NG_042310.1:g.10121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.682C>T MANE Select	ENSP00000292180.3:p.Arg228Cys
ENST00000292180.7:c.682C>T	ENSP00000292180.3:p.Arg228Cys
ENST00000295530.6:c.-120C>T	ENSP00000295530.2:n.-120C>T
ENST00000315144.14:c.391C>T	ENSP00000317296.10:p.Arg131Cys
ENST00000368431.7:c.385C>T	ENSP00000357416.3:p.Arg129Cys
ENST00000368432.5:c.391C>T	ENSP00000357417.1:p.Arg131Cys
ENST00000368433.5:c.682C>T	ENSP00000357418.1:p.Arg228Cys
ENST00000487371.1:n.738C>T
NM_001184891.1:c.391C>T	NP_001171820.1:p.Arg131Cys
NM_001184892.1:c.385C>T	NP_001171821.1:p.Arg129Cys
NM_025207.4:c.682C>T	NP_079483.3:p.Arg228Cys
NM_201398.2:c.391C>T	NP_958800.1:p.Arg131Cys
XM_005245502.2:c.391C>T	XP_005245559.1:p.Arg131Cys
XM_005245503.2:c.-120C>T	XP_005245560.1:n.-120C>T
XM_006711559.2:c.391C>T	XP_006711622.1:p.Arg131Cys
XR_241098.3:n.600C>T
NM_025207.5:c.682C>T MANE Select	NP_079483.3:p.Arg228Cys
NM_001184891.2:c.391C>T	NP_001171820.1:p.Arg131Cys
NM_001184892.2:c.385C>T	NP_001171821.1:p.Arg129Cys
NM_201398.3:c.391C>T	NP_958800.1:p.Arg131Cys