Canonical Allele Identifier: CA1604722958

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619492_180619494delinsCAG , CM000667.2:g.180619492_180619494delinsCAG	GRCh38
NC_000005.9:g.180046492_180046494delinsCAG , CM000667.1:g.180046492_180046494delinsCAG	GRCh37
NC_000005.8:g.179979098_179979100delinsCAG	NCBI36
NG_011536.1:g.35131_35133delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-128_2648-126delinsCTG MANE Select	ENSP00000261937.6:n.2648-128_2648-126delinsCTG
ENST00000261937.10:c.2648-128_2648-126delinsCTG	ENSP00000261937.6:n.2648-128_2648-126delinsCTG
ENST00000393347.7:c.2648-128_2648-126delinsCTG	ENSP00000377016.3:n.2648-128_2648-126delinsCTG
ENST00000502649.5:c.2648-128_2648-126delinsCTG	ENSP00000426057.1:n.2648-128_2648-126delinsCTG
ENST00000507059.5:n.1913_1915delinsCTG
ENST00000619105.4:c.*1591-128_*1591-126delinsCTG	ENSP00000481134.1:n.*1591-128_*1591-126delinsCTG
NM_002020.4:c.2648-128_2648-126delinsCTG	NP_002011.2:n.2648-128_2648-126delinsCTG
NM_182925.4:c.2648-128_2648-126delinsCTG	NP_891555.2:n.2648-128_2648-126delinsCTG
XM_011534477.1:c.2897-128_2897-126delinsCTG	XP_011532779.1:n.2897-128_2897-126delinsCTG
XM_011534478.1:c.2879-128_2879-126delinsCTG	XP_011532780.1:n.2879-128_2879-126delinsCTG
XM_011534479.1:c.2897-128_2897-126delinsCTG	XP_011532781.1:n.2897-128_2897-126delinsCTG
XM_011534480.1:c.2897-128_2897-126delinsCTG	XP_011532782.1:n.2897-128_2897-126delinsCTG
XM_011534481.1:c.2897-128_2897-126delinsCTG	XP_011532783.1:n.2897-128_2897-126delinsCTG
XM_011534482.1:c.2666-128_2666-126delinsCTG	XP_011532784.1:n.2666-128_2666-126delinsCTG
XM_011534483.1:c.2588-128_2588-126delinsCTG	XP_011532785.1:n.2588-128_2588-126delinsCTG
XM_011534484.1:c.2189-128_2189-126delinsCTG	XP_011532786.1:n.2189-128_2189-126delinsCTG
XR_941095.1:n.2909-128_2909-126delinsCTG
NM_001354989.1:c.2648-128_2648-126delinsCTG	NP_001341918.1:n.2648-128_2648-126delinsCTG
XM_011534478.3:c.2879-128_2879-126delinsCTG	XP_011532780.1:n.2879-128_2879-126delinsCTG
XM_011534484.2:c.2189-128_2189-126delinsCTG	XP_011532786.1:n.2189-128_2189-126delinsCTG
XM_017009263.1:c.2879-128_2879-126delinsCTG	XP_016864752.1:n.2879-128_2879-126delinsCTG
XM_017009264.2:c.2879-128_2879-126delinsCTG	XP_016864753.1:n.2879-128_2879-126delinsCTG
XM_017009265.1:c.2879-128_2879-126delinsCTG	XP_016864754.1:n.2879-128_2879-126delinsCTG
XM_017009266.1:c.2879-128_2879-126delinsCTG	XP_016864755.1:n.2879-128_2879-126delinsCTG
XM_017009267.2:c.2879-128_2879-126delinsCTG	XP_016864756.1:n.2879-128_2879-126delinsCTG
XM_017009268.1:c.2570-128_2570-126delinsCTG	XP_016864757.1:n.2570-128_2570-126delinsCTG
XR_001742050.2:n.3113-128_3113-126delinsCTG
NM_182925.5:c.2648-128_2648-126delinsCTG MANE Select	NP_891555.2:n.2648-128_2648-126delinsCTG
NM_001354989.2:c.2648-128_2648-126delinsCTG	NP_001341918.1:n.2648-128_2648-126delinsCTG
NM_002020.5:c.2648-128_2648-126delinsCTG	NP_002011.2:n.2648-128_2648-126delinsCTG