Canonical Allele Identifier: CA2676968858

Gene: FLT4

Linked Data

• gnomAD v4: 5-180609866-TGAGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609870_180609874del , CM000667.2:g.180609870_180609874del	GRCh38
NC_000005.9:g.180036870_180036874del , CM000667.1:g.180036870_180036874del	GRCh37
NC_000005.8:g.179969476_179969480del	NCBI36
NG_011536.1:g.44754_44758del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+34_3807+38del MANE Select	ENSP00000261937.6:n.3807+34_3807+38del
ENST00000261937.10:c.3807+34_3807+38del	ENSP00000261937.6:n.3807+34_3807+38del
ENST00000393347.7:c.3807+34_3807+38del	ENSP00000377016.3:n.3807+34_3807+38del
ENST00000502603.5:n.507+34_507+38del
ENST00000502649.5:c.3807+34_3807+38del	ENSP00000426057.1:n.3807+34_3807+38del
ENST00000507059.5:n.4191_4195del
ENST00000619105.4:c.*2750+34_*2750+38del	ENSP00000481134.1:n.*2750+34_*2750+38del
NM_002020.4:c.3807+34_3807+38del	NP_002011.2:n.3807+34_3807+38del
NM_182925.4:c.3807+34_3807+38del	NP_891555.2:n.3807+34_3807+38del
XM_011534477.1:c.4056+34_4056+38del	XP_011532779.1:n.4056+34_4056+38del
XM_011534478.1:c.4038+34_4038+38del	XP_011532780.1:n.4038+34_4038+38del
XM_011534479.1:c.4056+34_4056+38del	XP_011532781.1:n.4056+34_4056+38del
XM_011534480.1:c.4056+34_4056+38del	XP_011532782.1:n.4056+34_4056+38del
XM_011534481.1:c.4056+34_4056+38del	XP_011532783.1:n.4056+34_4056+38del
XM_011534482.1:c.3825+34_3825+38del	XP_011532784.1:n.3825+34_3825+38del
XM_011534483.1:c.3747+34_3747+38del	XP_011532785.1:n.3747+34_3747+38del
XM_011534484.1:c.3348+34_3348+38del	XP_011532786.1:n.3348+34_3348+38del
XR_941095.1:n.4093+34_4093+38del
NM_001354989.1:c.3807+34_3807+38del	NP_001341918.1:n.3807+34_3807+38del
XM_011534478.3:c.4038+34_4038+38del	XP_011532780.1:n.4038+34_4038+38del
XM_011534484.2:c.3348+34_3348+38del	XP_011532786.1:n.3348+34_3348+38del
XM_017009263.1:c.4038+34_4038+38del	XP_016864752.1:n.4038+34_4038+38del
XM_017009264.2:c.4038+34_4038+38del	XP_016864753.1:n.4038+34_4038+38del
XM_017009265.1:c.4038+34_4038+38del	XP_016864754.1:n.4038+34_4038+38del
XM_017009266.1:c.4038+34_4038+38del	XP_016864755.1:n.4038+34_4038+38del
XM_017009267.2:c.4038+34_4038+38del	XP_016864756.1:n.4038+34_4038+38del
XM_017009268.1:c.3729+34_3729+38del	XP_016864757.1:n.3729+34_3729+38del
XR_001742050.2:n.4297+34_4297+38del
NM_182925.5:c.3807+34_3807+38del MANE Select	NP_891555.2:n.3807+34_3807+38del
NM_001354989.2:c.3807+34_3807+38del	NP_001341918.1:n.3807+34_3807+38del
NM_002020.5:c.3807+34_3807+38del	NP_002011.2:n.3807+34_3807+38del