Canonical Allele Identifier: CA1134532

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154990202C>T , CM000663.2:g.154990202C>T	GRCh38
NC_000001.10:g.154962678C>T , CM000663.1:g.154962678C>T	GRCh37
NC_000001.9:g.153229302C>T	NCBI36
NG_042310.1:g.11909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.1309C>T MANE Select	ENSP00000292180.3:p.Arg437Cys
ENST00000292180.7:c.1309C>T	ENSP00000292180.3:p.Arg437Cys
ENST00000295530.6:c.360C>T	ENSP00000295530.2:p.Ser120=
ENST00000315144.14:c.1018C>T	ENSP00000317296.10:p.Arg340Cys
ENST00000368428.1:c.-150C>T	ENSP00000357413.1:n.-150C>T
ENST00000368432.5:c.1018C>T	ENSP00000357417.1:p.Arg340Cys
ENST00000368433.5:c.1309C>T	ENSP00000357418.1:p.Arg437Cys
ENST00000489992.5:n.309C>T
NM_001184891.1:c.1018C>T	NP_001171820.1:p.Arg340Cys
NM_025207.4:c.1309C>T	NP_079483.3:p.Arg437Cys
NM_201398.2:c.1018C>T	NP_958800.1:p.Arg340Cys
XM_005245502.2:c.1018C>T	XP_005245559.1:p.Arg340Cys
XM_005245503.2:c.508C>T	XP_005245560.1:p.Arg170Cys
XR_241098.3:n.1079C>T
NM_025207.5:c.1309C>T MANE Select	NP_079483.3:p.Arg437Cys
NM_001184891.2:c.1018C>T	NP_001171820.1:p.Arg340Cys
NM_201398.3:c.1018C>T	NP_958800.1:p.Arg340Cys