Canonical Allele Identifier: CA1134407
Community Standard Title: NM_025207.5(FLAD1):c.797A>G (p.Glu266Gly)
Gene: FLAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154988529A>G , CM000663.2:g.154988529A>G GRCh38
NC_000001.10:g.154961005A>G , CM000663.1:g.154961005A>G GRCh37
NC_000001.9:g.153227629A>G NCBI36
NG_042310.1:g.10236A>G

Transcript Alleles

HGVS Amino-acid Change
NM_025207.5:c.797A>G MANE Select NP_079483.3:p.Glu266Gly
ENST00000292180.8:c.797A>G MANE Select ENSP00000292180.3:p.Glu266Gly
NM_001184891.1:c.506A>G NP_001171820.1:p.Glu169Gly
NM_001184891.2:c.506A>G NP_001171820.1:p.Glu169Gly
NM_001184892.1:c.500A>G NP_001171821.1:p.Glu167Gly
NM_001184892.2:c.500A>G NP_001171821.1:p.Glu167Gly
NM_025207.4:c.797A>G NP_079483.3:p.Glu266Gly
NM_201398.2:c.506A>G NP_958800.1:p.Glu169Gly
NM_201398.3:c.506A>G NP_958800.1:p.Glu169Gly
ENST00000292180.7:c.797A>G ENSP00000292180.3:p.Glu266Gly
ENST00000295530.6:c.-5A>G ENSP00000295530.2:n.-5A>G
ENST00000315144.14:c.506A>G ENSP00000317296.10:p.Glu169Gly
ENST00000368431.7:c.500A>G ENSP00000357416.3:p.Glu167Gly
ENST00000368432.5:c.506A>G ENSP00000357417.1:p.Glu169Gly
ENST00000368433.5:c.797A>G ENSP00000357418.1:p.Glu266Gly
XM_005245502.2:c.506A>G XP_005245559.1:p.Glu169Gly
XM_005245503.2:c.-5A>G XP_005245560.1:n.-5A>G
XM_006711559.2:c.506A>G XP_006711622.1:p.Glu169Gly
XR_241098.3:n.715A>G