Canonical Allele Identifier: CA1134341

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988235A>G , CM000663.2:g.154988235A>G	GRCh38
NC_000001.10:g.154960711A>G , CM000663.1:g.154960711A>G	GRCh37
NC_000001.9:g.153227335A>G	NCBI36
NG_042310.1:g.9942A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025207.5:c.503A>G MANE Select	NP_079483.3:p.Asn168Ser
ENST00000292180.8:c.503A>G MANE Select	ENSP00000292180.3:p.Asn168Ser
NM_001184891.1:c.212A>G	NP_001171820.1:p.Asn71Ser
NM_001184891.2:c.212A>G	NP_001171820.1:p.Asn71Ser
NM_001184892.1:c.206A>G	NP_001171821.1:p.Asn69Ser
NM_001184892.2:c.206A>G	NP_001171821.1:p.Asn69Ser
NM_025207.4:c.503A>G	NP_079483.3:p.Asn168Ser
NM_201398.2:c.212A>G	NP_958800.1:p.Asn71Ser
NM_201398.3:c.212A>G	NP_958800.1:p.Asn71Ser
ENST00000292180.7:c.503A>G	ENSP00000292180.3:p.Asn168Ser
ENST00000295530.6:c.-299A>G	ENSP00000295530.2:n.-299A>G
ENST00000315144.14:c.212A>G	ENSP00000317296.10:p.Asn71Ser
ENST00000368431.7:c.206A>G	ENSP00000357416.3:p.Asn69Ser
ENST00000368432.5:c.212A>G	ENSP00000357417.1:p.Asn71Ser
ENST00000368433.5:c.503A>G	ENSP00000357418.1:p.Asn168Ser
ENST00000487371.1:n.559A>G
XM_005245502.2:c.212A>G	XP_005245559.1:p.Asn71Ser
XM_005245503.2:c.-299A>G	XP_005245560.1:n.-299A>G
XM_006711559.2:c.212A>G	XP_006711622.1:p.Asn71Ser
XR_241098.3:n.421A>G