Canonical Allele Identifier: CA2676968595

Gene: FLT4

Linked Data

• gnomAD v4: 5-180609580-TGGGGCCCCTCTGCCCAGCGCTCACTGACCAGGCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609584_180609618del , CM000667.2:g.180609584_180609618del	GRCh38
NC_000005.9:g.180036584_180036618del , CM000667.1:g.180036584_180036618del	GRCh37
NC_000005.8:g.179969190_179969224del	NCBI36
NG_011536.1:g.45010_45044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+290_3807+324del MANE Select	ENSP00000261937.6:n.3807+290_3807+324del
ENST00000261937.10:c.3807+290_3807+324del	ENSP00000261937.6:n.3807+290_3807+324del
ENST00000393347.7:c.3807+290_3807+324del	ENSP00000377016.3:n.3807+290_3807+324del
ENST00000502603.5:n.507+290_507+324del
ENST00000502649.5:c.3807+290_3807+324del	ENSP00000426057.1:n.3807+290_3807+324del
ENST00000507059.5:n.4447_4481del
ENST00000619105.4:c.*2750+290_*2750+324del	ENSP00000481134.1:n.*2750+290_*2750+324del
NM_002020.4:c.3807+290_3807+324del	NP_002011.2:n.3807+290_3807+324del
NM_182925.4:c.3807+290_3807+324del	NP_891555.2:n.3807+290_3807+324del
XM_011534477.1:c.4056+290_4056+324del	XP_011532779.1:n.4056+290_4056+324del
XM_011534478.1:c.4038+290_4038+324del	XP_011532780.1:n.4038+290_4038+324del
XM_011534479.1:c.4056+290_4056+324del	XP_011532781.1:n.4056+290_4056+324del
XM_011534480.1:c.4056+290_4056+324del	XP_011532782.1:n.4056+290_4056+324del
XM_011534481.1:c.4056+290_4056+324del	XP_011532783.1:n.4056+290_4056+324del
XM_011534482.1:c.3825+290_3825+324del	XP_011532784.1:n.3825+290_3825+324del
XM_011534483.1:c.3747+290_3747+324del	XP_011532785.1:n.3747+290_3747+324del
XM_011534484.1:c.3348+290_3348+324del	XP_011532786.1:n.3348+290_3348+324del
XR_941095.1:n.4093+290_4093+324del
NM_001354989.1:c.3807+290_3807+324del	NP_001341918.1:n.3807+290_3807+324del
XM_011534478.3:c.4038+290_4038+324del	XP_011532780.1:n.4038+290_4038+324del
XM_011534484.2:c.3348+290_3348+324del	XP_011532786.1:n.3348+290_3348+324del
XM_017009263.1:c.4038+290_4038+324del	XP_016864752.1:n.4038+290_4038+324del
XM_017009264.2:c.4038+290_4038+324del	XP_016864753.1:n.4038+290_4038+324del
XM_017009265.1:c.4038+290_4038+324del	XP_016864754.1:n.4038+290_4038+324del
XM_017009266.1:c.4038+290_4038+324del	XP_016864755.1:n.4038+290_4038+324del
XM_017009267.2:c.4038+290_4038+324del	XP_016864756.1:n.4038+290_4038+324del
XM_017009268.1:c.3729+290_3729+324del	XP_016864757.1:n.3729+290_3729+324del
XR_001742050.2:n.4297+290_4297+324del
NM_182925.5:c.3807+290_3807+324del MANE Select	NP_891555.2:n.3807+290_3807+324del
NM_001354989.2:c.3807+290_3807+324del	NP_001341918.1:n.3807+290_3807+324del
NM_002020.5:c.3807+290_3807+324del	NP_002011.2:n.3807+290_3807+324del