Canonical Allele Identifier: CA1143690619

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154992694T= , CM000663.2:g.154992694T=	GRCh38
NC_000001.10:g.154965170T= , CM000663.1:g.154965170T=	GRCh37
NC_000001.9:g.153231794T=	NCBI36
NG_042310.1:g.14401T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.1555-19T= MANE Select	ENSP00000292180.3:n.1555-19T=
ENST00000292180.7:c.1555-19T=	ENSP00000292180.3:n.1555-19T=
ENST00000295530.6:c.*11+21T=	ENSP00000295530.2:n.*11+21T=
ENST00000315144.14:c.1264-19T=	ENSP00000317296.10:n.1264-19T=
ENST00000368428.1:c.178-19T=	ENSP00000357413.1:n.178-19T=
ENST00000368432.5:c.1264-19T=	ENSP00000357417.1:n.1264-19T=
ENST00000477609.5:n.344+21T=
ENST00000481758.1:n.106T=
ENST00000489992.5:n.365-19T=
NM_001184891.1:c.1264-19T=	NP_001171820.1:n.1264-19T=
NM_025207.4:c.1555-19T=	NP_079483.3:n.1555-19T=
NM_201398.2:c.1264-19T=	NP_958800.1:n.1264-19T=
XM_005245502.2:c.*103T=	XP_005245559.1:n.*103T=
XM_005245503.2:c.754-19T=	XP_005245560.1:n.754-19T=
XR_241098.3:n.1325-19T=
NM_025207.5:c.1555-19T= MANE Select	NP_079483.3:n.1555-19T=
NM_001184891.2:c.1264-19T=	NP_001171820.1:n.1264-19T=
NM_201398.3:c.1264-19T=	NP_958800.1:n.1264-19T=