Canonical Allele Identifier: CA2481098875

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992746C= , CM000663.2:g.154992746C=	GRCh38
NC_000001.10:g.154965222C= , CM000663.1:g.154965222C=	GRCh37
NC_000001.9:g.153231846C=	NCBI36
NG_042310.1:g.14453C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000292180.8:c.1588C= MANE Select	ENSP00000292180.3:p.Arg530=
ENST00000292180.7:c.1588C=	ENSP00000292180.3:p.Arg530=
ENST00000295530.6:c.*11+73C=	ENSP00000295530.2:n.*11+73C=
ENST00000315144.14:c.1297C=	ENSP00000317296.10:p.Arg433=
ENST00000368428.1:c.211C=	ENSP00000357413.1:p.Arg71=
ENST00000368432.5:c.1297C=	ENSP00000357417.1:p.Arg433=
ENST00000477609.5:n.344+73C=
ENST00000481758.1:n.158C=
ENST00000489992.5:n.398C=
NM_001184891.1:c.1297C=	NP_001171820.1:p.Arg433=
NM_025207.4:c.1588C=	NP_079483.3:p.Arg530=
NM_201398.2:c.1297C=	NP_958800.1:p.Arg433=
XM_005245503.2:c.787C=	XP_005245560.1:p.Arg263=
XR_241098.3:n.1358C=
NM_025207.5:c.1588C= MANE Select	NP_079483.3:p.Arg530=
NM_001184891.2:c.1297C=	NP_001171820.1:p.Arg433=
NM_201398.3:c.1297C=	NP_958800.1:p.Arg433=