Canonical Allele Identifier: CA257470
Gene: FLT4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16266
ClinVar RCV Id: RCV000017654
dbSNP Id: rs121909655

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180614142A>G , CM000667.2:g.180614142A>G GRCh38
NC_000005.8:g.179973748A>G NCBI36
NC_000005.9:g.180041142A>G , CM000667.1:g.180041142A>G GRCh37
NG_011536.1:g.40483T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261937.10:c.3257T>C ENSP00000261937.6:p.Ile1086Thr
ENST00000393347.7:c.3257T>C ENSP00000377016.3:p.Ile1086Thr
ENST00000502649.5:c.3257T>C ENSP00000426057.1:p.Ile1086Thr
ENST00000507059.5:n.2650T>C
ENST00000512795.1:c.371T>C ENSP00000421535.1:p.Ile124Thr
ENST00000514810.1:n.624T>C
ENST00000619105.4:c.*2200T>C ENSP00000481134.1:p.=
NM_002020.4:c.3257T>C VV NP_002011.2:p.Ile1086Thr
NM_182925.4:c.3257T>C VV NP_891555.2:p.Ile1086Thr
XM_011534477.1:c.3506T>C XP_011532779.1:p.Ile1169Thr
XM_011534478.1:c.3488T>C XP_011532780.1:p.Ile1163Thr
XM_011534479.1:c.3506T>C XP_011532781.1:p.Ile1169Thr
XM_011534480.1:c.3506T>C XP_011532782.1:p.Ile1169Thr
XM_011534481.1:c.3506T>C XP_011532783.1:p.Ile1169Thr
XM_011534482.1:c.3275T>C XP_011532784.1:p.Ile1092Thr
XM_011534483.1:c.3197T>C XP_011532785.1:p.Ile1066Thr
XM_011534484.1:c.2798T>C XP_011532786.1:p.Ile933Thr
XR_941095.1:n.3518T>C