Canonical Allele Identifier: CA133199081

Gene: FLT4

Linked Data

• dbSNP Id: rs34649813
• MyVariant Identifiers: chr5:g.180036483_180036484insT (hg19) ; chr5:g.180609483_180609484insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609483_180609484insT , CM000667.2:g.180609483_180609484insT	GRCh38
NC_000005.9:g.180036483_180036484insT , CM000667.1:g.180036483_180036484insT	GRCh37
NC_000005.8:g.179969089_179969090insT	NCBI36
NG_011536.1:g.45141_45142insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+421_3807+422insA MANE Select	ENSP00000261937.6:n.3807+421_3807+422insA
ENST00000261937.10:c.3807+421_3807+422insA	ENSP00000261937.6:n.3807+421_3807+422insA
ENST00000393347.7:c.3807+421_3807+422insA	ENSP00000377016.3:n.3807+421_3807+422insA
ENST00000502603.5:n.507+421_507+422insA
ENST00000502649.5:c.3807+421_3807+422insA	ENSP00000426057.1:n.3807+421_3807+422insA
ENST00000507059.5:n.4578_4579insA
ENST00000619105.4:c.*2750+421_*2750+422insA	ENSP00000481134.1:n.*2750+421_*2750+422insA
NM_002020.4:c.3807+421_3807+422insA	NP_002011.2:n.3807+421_3807+422insA
NM_182925.4:c.3807+421_3807+422insA	NP_891555.2:n.3807+421_3807+422insA
XM_011534477.1:c.4056+421_4056+422insA	XP_011532779.1:n.4056+421_4056+422insA
XM_011534478.1:c.4038+421_4038+422insA	XP_011532780.1:n.4038+421_4038+422insA
XM_011534479.1:c.4057-253_4057-252insA	XP_011532781.1:n.4057-253_4057-252insA
XM_011534480.1:c.4057-253_4057-252insA	XP_011532782.1:n.4057-253_4057-252insA
XM_011534481.1:c.4056+421_4056+422insA	XP_011532783.1:n.4056+421_4056+422insA
XM_011534482.1:c.3825+421_3825+422insA	XP_011532784.1:n.3825+421_3825+422insA
XM_011534483.1:c.3747+421_3747+422insA	XP_011532785.1:n.3747+421_3747+422insA
XM_011534484.1:c.3348+421_3348+422insA	XP_011532786.1:n.3348+421_3348+422insA
XR_941095.1:n.4093+421_4093+422insA
NM_001354989.1:c.3807+421_3807+422insA	NP_001341918.1:n.3807+421_3807+422insA
XM_011534478.3:c.4038+421_4038+422insA	XP_011532780.1:n.4038+421_4038+422insA
XM_011534484.2:c.3348+421_3348+422insA	XP_011532786.1:n.3348+421_3348+422insA
XM_017009263.1:c.4039-253_4039-252insA	XP_016864752.1:n.4039-253_4039-252insA
XM_017009264.2:c.4039-253_4039-252insA	XP_016864753.1:n.4039-253_4039-252insA
XM_017009265.1:c.4039-253_4039-252insA	XP_016864754.1:n.4039-253_4039-252insA
XM_017009266.1:c.4038+421_4038+422insA	XP_016864755.1:n.4038+421_4038+422insA
XM_017009267.2:c.4038+421_4038+422insA	XP_016864756.1:n.4038+421_4038+422insA
XM_017009268.1:c.3729+421_3729+422insA	XP_016864757.1:n.3729+421_3729+422insA
XR_001742050.2:n.4297+421_4297+422insA
NM_182925.5:c.3807+421_3807+422insA MANE Select	NP_891555.2:n.3807+421_3807+422insA
NM_001354989.2:c.3807+421_3807+422insA	NP_001341918.1:n.3807+421_3807+422insA
NM_002020.5:c.3807+421_3807+422insA	NP_002011.2:n.3807+421_3807+422insA