Canonical Allele Identifier: CA342742256
Gene: FLAD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154988153T>G , CM000663.2:g.154988153T>G GRCh38
NC_000001.10:g.154960629T>G , CM000663.1:g.154960629T>G GRCh37
NC_000001.9:g.153227253T>G NCBI36
NG_042310.1:g.9860T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000292180.8:c.421T>G MANE Select ENSP00000292180.3:p.Ser141Ala
ENST00000292180.7:c.421T>G ENSP00000292180.3:p.Ser141Ala
ENST00000295530.6:c.-381T>G ENSP00000295530.2:n.-381T>G
ENST00000315144.14:c.130T>G ENSP00000317296.10:p.Ser44Ala
ENST00000368431.7:c.124T>G ENSP00000357416.3:p.Ser42Ala
ENST00000368432.5:c.130T>G ENSP00000357417.1:p.Ser44Ala
ENST00000368433.5:c.421T>G ENSP00000357418.1:p.Ser141Ala
ENST00000487371.1:n.477T>G
NM_001184891.1:c.130T>G NP_001171820.1:p.Ser44Ala
NM_001184892.1:c.124T>G NP_001171821.1:p.Ser42Ala
NM_025207.4:c.421T>G NP_079483.3:p.Ser141Ala
NM_201398.2:c.130T>G NP_958800.1:p.Ser44Ala
XM_005245502.2:c.130T>G XP_005245559.1:p.Ser44Ala
XM_005245503.2:c.-381T>G XP_005245560.1:n.-381T>G
XM_006711559.2:c.130T>G XP_006711622.1:p.Ser44Ala
XR_241098.3:n.339T>G
NM_025207.5:c.421T>G MANE Select NP_079483.3:p.Ser141Ala
NM_001184891.2:c.130T>G NP_001171820.1:p.Ser44Ala
NM_001184892.2:c.124T>G NP_001171821.1:p.Ser42Ala
NM_201398.3:c.130T>G NP_958800.1:p.Ser44Ala