Canonical Allele Identifier: CA1604717299

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609607_180609613delinsACCAGGC , CM000667.2:g.180609607_180609613delinsACCAGGC	GRCh38
NC_000005.9:g.180036607_180036613delinsACCAGGC , CM000667.1:g.180036607_180036613delinsACCAGGC	GRCh37
NC_000005.8:g.179969213_179969219delinsACCAGGC	NCBI36
NG_011536.1:g.45012_45018delinsGCCTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+292_3807+298delinsGCCTGGT MANE Select	ENSP00000261937.6:n.3807+292_3807+298delinsGCCTGGT
ENST00000261937.10:c.3807+292_3807+298delinsGCCTGGT	ENSP00000261937.6:n.3807+292_3807+298delinsGCCTGGT
ENST00000393347.7:c.3807+292_3807+298delinsGCCTGGT	ENSP00000377016.3:n.3807+292_3807+298delinsGCCTGGT
ENST00000502603.5:n.507+292_507+298delinsGCCTGGT
ENST00000502649.5:c.3807+292_3807+298delinsGCCTGGT	ENSP00000426057.1:n.3807+292_3807+298delinsGCCTGGT
ENST00000507059.5:n.4449_4455delinsGCCTGGT
ENST00000619105.4:c.*2750+292_*2750+298delinsGCCTGGT	ENSP00000481134.1:n.*2750+292_*2750+298delinsGCCTGGT
NM_002020.4:c.3807+292_3807+298delinsGCCTGGT	NP_002011.2:n.3807+292_3807+298delinsGCCTGGT
NM_182925.4:c.3807+292_3807+298delinsGCCTGGT	NP_891555.2:n.3807+292_3807+298delinsGCCTGGT
XM_011534477.1:c.4056+292_4056+298delinsGCCTGGT	XP_011532779.1:n.4056+292_4056+298delinsGCCTGGT
XM_011534478.1:c.4038+292_4038+298delinsGCCTGGT	XP_011532780.1:n.4038+292_4038+298delinsGCCTGGT
XM_011534479.1:c.4056+292_4056+298delinsGCCTGGT	XP_011532781.1:n.4056+292_4056+298delinsGCCTGGT
XM_011534480.1:c.4056+292_4056+298delinsGCCTGGT	XP_011532782.1:n.4056+292_4056+298delinsGCCTGGT
XM_011534481.1:c.4056+292_4056+298delinsGCCTGGT	XP_011532783.1:n.4056+292_4056+298delinsGCCTGGT
XM_011534482.1:c.3825+292_3825+298delinsGCCTGGT	XP_011532784.1:n.3825+292_3825+298delinsGCCTGGT
XM_011534483.1:c.3747+292_3747+298delinsGCCTGGT	XP_011532785.1:n.3747+292_3747+298delinsGCCTGGT
XM_011534484.1:c.3348+292_3348+298delinsGCCTGGT	XP_011532786.1:n.3348+292_3348+298delinsGCCTGGT
XR_941095.1:n.4093+292_4093+298delinsGCCTGGT
NM_001354989.1:c.3807+292_3807+298delinsGCCTGGT	NP_001341918.1:n.3807+292_3807+298delinsGCCTGGT
XM_011534478.3:c.4038+292_4038+298delinsGCCTGGT	XP_011532780.1:n.4038+292_4038+298delinsGCCTGGT
XM_011534484.2:c.3348+292_3348+298delinsGCCTGGT	XP_011532786.1:n.3348+292_3348+298delinsGCCTGGT
XM_017009263.1:c.4038+292_4038+298delinsGCCTGGT	XP_016864752.1:n.4038+292_4038+298delinsGCCTGGT
XM_017009264.2:c.4038+292_4038+298delinsGCCTGGT	XP_016864753.1:n.4038+292_4038+298delinsGCCTGGT
XM_017009265.1:c.4038+292_4038+298delinsGCCTGGT	XP_016864754.1:n.4038+292_4038+298delinsGCCTGGT
XM_017009266.1:c.4038+292_4038+298delinsGCCTGGT	XP_016864755.1:n.4038+292_4038+298delinsGCCTGGT
XM_017009267.2:c.4038+292_4038+298delinsGCCTGGT	XP_016864756.1:n.4038+292_4038+298delinsGCCTGGT
XM_017009268.1:c.3729+292_3729+298delinsGCCTGGT	XP_016864757.1:n.3729+292_3729+298delinsGCCTGGT
XR_001742050.2:n.4297+292_4297+298delinsGCCTGGT
NM_182925.5:c.3807+292_3807+298delinsGCCTGGT MANE Select	NP_891555.2:n.3807+292_3807+298delinsGCCTGGT
NM_001354989.2:c.3807+292_3807+298delinsGCCTGGT	NP_001341918.1:n.3807+292_3807+298delinsGCCTGGT
NM_002020.5:c.3807+292_3807+298delinsGCCTGGT	NP_002011.2:n.3807+292_3807+298delinsGCCTGGT