Canonical Allele Identifier: CA342741069
Gene: FLAD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154988045T>C , CM000663.2:g.154988045T>C GRCh38
NC_000001.10:g.154960521T>C , CM000663.1:g.154960521T>C GRCh37
NC_000001.9:g.153227145T>C NCBI36
NG_042310.1:g.9752T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292180.8:c.373-60T>C MANE Select ENSP00000292180.3:n.373-60T>C
ENST00000292180.7:c.373-60T>C ENSP00000292180.3:n.373-60T>C
ENST00000315144.14:c.82-60T>C ENSP00000317296.10:n.82-60T>C
ENST00000368431.7:c.16T>C ENSP00000357416.3:p.Ser6Pro
ENST00000368432.5:c.82-60T>C ENSP00000357417.1:n.82-60T>C
ENST00000368433.5:c.373-60T>C ENSP00000357418.1:n.373-60T>C
ENST00000487371.1:n.429-60T>C
ENST00000492620.1:n.640T>C
NM_001184891.1:c.82-60T>C NP_001171820.1:n.82-60T>C
NM_001184892.1:c.16T>C NP_001171821.1:p.Ser6Pro
NM_025207.4:c.373-60T>C NP_079483.3:n.373-60T>C
NM_201398.2:c.82-60T>C NP_958800.1:n.82-60T>C
XM_005245502.2:c.82-60T>C XP_005245559.1:n.82-60T>C
XM_005245503.2:c.-429-60T>C XP_005245560.1:n.-429-60T>C
XM_006711559.2:c.82-60T>C XP_006711622.1:n.82-60T>C
XR_241098.3:n.291-60T>C
NM_025207.5:c.373-60T>C MANE Select NP_079483.3:n.373-60T>C
NM_001184891.2:c.82-60T>C NP_001171820.1:n.82-60T>C
NM_001184892.2:c.16T>C NP_001171821.1:p.Ser6Pro
NM_201398.3:c.82-60T>C NP_958800.1:n.82-60T>C