Canonical Allele Identifier: CA1604717441
Gene: FLT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609881_180609882delinsGC , CM000667.2:g.180609881_180609882delinsGC GRCh38
NC_000005.9:g.180036881_180036882delinsGC , CM000667.1:g.180036881_180036882delinsGC GRCh37
NC_000005.8:g.179969487_179969488delinsGC NCBI36
NG_011536.1:g.44743_44744delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3807+23_3807+24delinsGC MANE Select ENSP00000261937.6:n.3807+23_3807+24delinsGC
ENST00000261937.10:c.3807+23_3807+24delinsGC ENSP00000261937.6:n.3807+23_3807+24delinsGC
ENST00000393347.7:c.3807+23_3807+24delinsGC ENSP00000377016.3:n.3807+23_3807+24delinsGC
ENST00000502603.5:n.507+23_507+24delinsGC
ENST00000502649.5:c.3807+23_3807+24delinsGC ENSP00000426057.1:n.3807+23_3807+24delinsGC
ENST00000507059.5:n.4180_4181delinsGC
ENST00000619105.4:c.*2750+23_*2750+24delinsGC ENSP00000481134.1:n.*2750+23_*2750+24delinsGC
NM_002020.4:c.3807+23_3807+24delinsGC NP_002011.2:n.3807+23_3807+24delinsGC
NM_182925.4:c.3807+23_3807+24delinsGC NP_891555.2:n.3807+23_3807+24delinsGC
XM_011534477.1:c.4056+23_4056+24delinsGC XP_011532779.1:n.4056+23_4056+24delinsGC
XM_011534478.1:c.4038+23_4038+24delinsGC XP_011532780.1:n.4038+23_4038+24delinsGC
XM_011534479.1:c.4056+23_4056+24delinsGC XP_011532781.1:n.4056+23_4056+24delinsGC
XM_011534480.1:c.4056+23_4056+24delinsGC XP_011532782.1:n.4056+23_4056+24delinsGC
XM_011534481.1:c.4056+23_4056+24delinsGC XP_011532783.1:n.4056+23_4056+24delinsGC
XM_011534482.1:c.3825+23_3825+24delinsGC XP_011532784.1:n.3825+23_3825+24delinsGC
XM_011534483.1:c.3747+23_3747+24delinsGC XP_011532785.1:n.3747+23_3747+24delinsGC
XM_011534484.1:c.3348+23_3348+24delinsGC XP_011532786.1:n.3348+23_3348+24delinsGC
XR_941095.1:n.4093+23_4093+24delinsGC
NM_001354989.1:c.3807+23_3807+24delinsGC NP_001341918.1:n.3807+23_3807+24delinsGC
XM_011534478.3:c.4038+23_4038+24delinsGC XP_011532780.1:n.4038+23_4038+24delinsGC
XM_011534484.2:c.3348+23_3348+24delinsGC XP_011532786.1:n.3348+23_3348+24delinsGC
XM_017009263.1:c.4038+23_4038+24delinsGC XP_016864752.1:n.4038+23_4038+24delinsGC
XM_017009264.2:c.4038+23_4038+24delinsGC XP_016864753.1:n.4038+23_4038+24delinsGC
XM_017009265.1:c.4038+23_4038+24delinsGC XP_016864754.1:n.4038+23_4038+24delinsGC
XM_017009266.1:c.4038+23_4038+24delinsGC XP_016864755.1:n.4038+23_4038+24delinsGC
XM_017009267.2:c.4038+23_4038+24delinsGC XP_016864756.1:n.4038+23_4038+24delinsGC
XM_017009268.1:c.3729+23_3729+24delinsGC XP_016864757.1:n.3729+23_3729+24delinsGC
XR_001742050.2:n.4297+23_4297+24delinsGC
NM_182925.5:c.3807+23_3807+24delinsGC MANE Select NP_891555.2:n.3807+23_3807+24delinsGC
NM_001354989.2:c.3807+23_3807+24delinsGC NP_001341918.1:n.3807+23_3807+24delinsGC
NM_002020.5:c.3807+23_3807+24delinsGC NP_002011.2:n.3807+23_3807+24delinsGC