Canonical Allele Identifier: CA257467
Gene: FLT4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16262
ClinVar RCV Id: RCV000017650
dbSNP Id: rs121909652

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180613101G>A , CM000667.2:g.180613101G>A GRCh38
NC_000005.9:g.180040101G>A , CM000667.1:g.180040101G>A GRCh37
NC_000005.8:g.179972707G>A NCBI36
NG_011536.1:g.41524C>T

Transcript Alleles

HGVS Amino-acid change
NM_002020.4:c.3341C>T VV NP_002011.2:p.Pro1114Leu
NM_182925.4:c.3341C>T VV NP_891555.2:p.Pro1114Leu
XM_011534477.1:c.3590C>T XP_011532779.1:p.Pro1197Leu
XM_011534478.1:c.3572C>T XP_011532780.1:p.Pro1191Leu
XM_011534479.1:c.3590C>T XP_011532781.1:p.Pro1197Leu
XM_011534480.1:c.3590C>T XP_011532782.1:p.Pro1197Leu
XM_011534481.1:c.3590C>T XP_011532783.1:p.Pro1197Leu
XM_011534482.1:c.3359C>T XP_011532784.1:p.Pro1120Leu
XM_011534483.1:c.3281C>T XP_011532785.1:p.Pro1094Leu
XM_011534484.1:c.2882C>T XP_011532786.1:p.Pro961Leu
XR_941095.1:n.3602C>T
NM_001354989.1:c.3341C>T VV NP_001341918.1:p.Pro1114Leu
XM_011534478.3:c.3572C>T XP_011532780.1:p.Pro1191Leu
XM_011534484.2:c.2882C>T XP_011532786.1:p.Pro961Leu
XM_017009263.1:c.3572C>T XP_016864752.1:p.Pro1191Leu
XM_017009264.2:c.3572C>T XP_016864753.1:p.Pro1191Leu
XM_017009265.1:c.3572C>T XP_016864754.1:p.Pro1191Leu
XM_017009266.1:c.3572C>T XP_016864755.1:p.Pro1191Leu
XM_017009267.2:c.3572C>T XP_016864756.1:p.Pro1191Leu
XM_017009268.1:c.3263C>T XP_016864757.1:p.Pro1088Leu
XR_001742050.2:n.3806C>T
NM_182925.5:c.3341C>T VV MANE Preferred NP_891555.2:p.Pro1114Leu
ENST00000261937.10:c.3341C>T ENSP00000261937.6:p.Pro1114Leu
ENST00000393347.7:c.3341C>T ENSP00000377016.3:p.Pro1114Leu
ENST00000502649.5:c.3341C>T ENSP00000426057.1:p.Pro1114Leu
ENST00000507059.5:n.3691C>T
ENST00000510000.1:n.293C>T
ENST00000619105.4:c.*2284C>T ENSP00000481134.1:p.=