Canonical Allele Identifier: CA1134257
Gene: FLAD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154983910C>T , CM000663.2:g.154983910C>T GRCh38
NC_000001.10:g.154956386C>T , CM000663.1:g.154956386C>T GRCh37
NC_000001.9:g.153223010C>T NCBI36
NG_042310.1:g.5617C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025207.5:c.216C>T MANE Select NP_079483.3:p.Pro72=
ENST00000292180.8:c.216C>T MANE Select ENSP00000292180.3:p.Pro72=
NM_001184891.1:c.-76C>T NP_001171820.1:n.-76C>T
NM_001184891.2:c.-76C>T NP_001171820.1:n.-76C>T
NM_001184892.1:c.-721C>T NP_001171821.1:n.-721C>T
NM_001184892.2:c.-721C>T NP_001171821.1:n.-721C>T
NM_025207.4:c.216C>T NP_079483.3:p.Pro72=
NM_201398.2:c.-76C>T NP_958800.1:n.-76C>T
NM_201398.3:c.-76C>T NP_958800.1:n.-76C>T
ENST00000292180.7:c.216C>T ENSP00000292180.3:p.Pro72=
ENST00000315144.14:c.-76C>T ENSP00000317296.10:n.-76C>T
ENST00000368431.7:c.-721C>T ENSP00000357416.3:n.-721C>T
ENST00000368432.5:c.-76C>T ENSP00000357417.1:n.-76C>T
ENST00000368433.5:c.216C>T ENSP00000357418.1:p.Pro72=
ENST00000487371.1:n.272C>T
ENST00000492620.1:n.60+513C>T
XM_005245502.2:c.-76C>T XP_005245559.1:n.-76C>T
XM_005245503.2:c.-430+513C>T XP_005245560.1:n.-430+513C>T
XM_006711559.2:c.-76C>T XP_006711622.1:n.-76C>T
XR_241098.3:n.134C>T