Canonical Allele Identifier: CA1148278739

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992669G= , CM000663.2:g.154992669G=	GRCh38
NC_000001.10:g.154965145G= , CM000663.1:g.154965145G=	GRCh37
NC_000001.9:g.153231769G=	NCBI36
NG_042310.1:g.14376G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.1555-44G= MANE Select	ENSP00000292180.3:n.1555-44G=
ENST00000292180.7:c.1555-44G=	ENSP00000292180.3:n.1555-44G=
ENST00000295530.6:c.*7G=	ENSP00000295530.2:n.*7G=
ENST00000315144.14:c.1264-44G=	ENSP00000317296.10:n.1264-44G=
ENST00000368428.1:c.178-44G=	ENSP00000357413.1:n.178-44G=
ENST00000368432.5:c.1264-44G=	ENSP00000357417.1:n.1264-44G=
ENST00000477609.5:n.340G=
ENST00000481758.1:n.81G=
ENST00000489992.5:n.365-44G=
NM_001184891.1:c.1264-44G=	NP_001171820.1:n.1264-44G=
NM_025207.4:c.1555-44G=	NP_079483.3:n.1555-44G=
NM_201398.2:c.1264-44G=	NP_958800.1:n.1264-44G=
XM_005245502.2:c.*78G=	XP_005245559.1:n.*78G=
XM_005245503.2:c.754-44G=	XP_005245560.1:n.754-44G=
XR_241098.3:n.1325-44G=
NM_025207.5:c.1555-44G= MANE Select	NP_079483.3:n.1555-44G=
NM_001184891.2:c.1264-44G=	NP_001171820.1:n.1264-44G=
NM_201398.3:c.1264-44G=	NP_958800.1:n.1264-44G=