Canonical Allele Identifier: CA1134410

Gene: FLAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154988535T>G , CM000663.2:g.154988535T>G	GRCh38
NC_000001.10:g.154961011T>G , CM000663.1:g.154961011T>G	GRCh37
NC_000001.9:g.153227635T>G	NCBI36
NG_042310.1:g.10242T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292180.8:c.803T>G MANE Select	ENSP00000292180.3:p.Met268Arg
ENST00000292180.7:c.803T>G	ENSP00000292180.3:p.Met268Arg
ENST00000295530.6:c.2T>G	ENSP00000295530.2:p.Met1Arg
ENST00000315144.14:c.512T>G	ENSP00000317296.10:p.Met171Arg
ENST00000368431.7:c.506T>G	ENSP00000357416.3:p.Met169Arg
ENST00000368432.5:c.512T>G	ENSP00000357417.1:p.Met171Arg
ENST00000368433.5:c.803T>G	ENSP00000357418.1:p.Met268Arg
NM_001184891.1:c.512T>G	NP_001171820.1:p.Met171Arg
NM_001184892.1:c.506T>G	NP_001171821.1:p.Met169Arg
NM_025207.4:c.803T>G	NP_079483.3:p.Met268Arg
NM_201398.2:c.512T>G	NP_958800.1:p.Met171Arg
XM_005245502.2:c.512T>G	XP_005245559.1:p.Met171Arg
XM_005245503.2:c.2T>G	XP_005245560.1:p.Met1Arg
XM_006711559.2:c.512T>G	XP_006711622.1:p.Met171Arg
XR_241098.3:n.721T>G
NM_025207.5:c.803T>G MANE Select	NP_079483.3:p.Met268Arg
NM_001184891.2:c.512T>G	NP_001171820.1:p.Met171Arg
NM_001184892.2:c.506T>G	NP_001171821.1:p.Met169Arg
NM_201398.3:c.512T>G	NP_958800.1:p.Met171Arg