Canonical Allele Identifier: CA421237063

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988257A>G , CM000663.2:g.154988257A>G	GRCh38
NC_000001.10:g.154960733A>G , CM000663.1:g.154960733A>G	GRCh37
NC_000001.9:g.153227357A>G	NCBI36
NG_042310.1:g.9964A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.525A>G MANE Select	ENSP00000292180.3:p.Thr175=
ENST00000292180.7:c.525A>G	ENSP00000292180.3:p.Thr175=
ENST00000295530.6:c.-277A>G	ENSP00000295530.2:n.-277A>G
ENST00000315144.14:c.234A>G	ENSP00000317296.10:p.Thr78=
ENST00000368431.7:c.228A>G	ENSP00000357416.3:p.Thr76=
ENST00000368432.5:c.234A>G	ENSP00000357417.1:p.Thr78=
ENST00000368433.5:c.525A>G	ENSP00000357418.1:p.Thr175=
ENST00000487371.1:n.581A>G
NM_001184891.1:c.234A>G	NP_001171820.1:p.Thr78=
NM_001184892.1:c.228A>G	NP_001171821.1:p.Thr76=
NM_025207.4:c.525A>G	NP_079483.3:p.Thr175=
NM_201398.2:c.234A>G	NP_958800.1:p.Thr78=
XM_005245502.2:c.234A>G	XP_005245559.1:p.Thr78=
XM_005245503.2:c.-277A>G	XP_005245560.1:n.-277A>G
XM_006711559.2:c.234A>G	XP_006711622.1:p.Thr78=
XR_241098.3:n.443A>G
NM_025207.5:c.525A>G MANE Select	NP_079483.3:p.Thr175=
NM_001184891.2:c.234A>G	NP_001171820.1:p.Thr78=
NM_001184892.2:c.228A>G	NP_001171821.1:p.Thr76=
NM_201398.3:c.234A>G	NP_958800.1:p.Thr78=