Canonical Allele Identifier: CA1604717239

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609486G= , CM000667.2:g.180609486G=	GRCh38
NC_000005.9:g.180036486G= , CM000667.1:g.180036486G=	GRCh37
NC_000005.8:g.179969092G=	NCBI36
NG_011536.1:g.45139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3807+419C= MANE Select	ENSP00000261937.6:n.3807+419C=
ENST00000261937.10:c.3807+419C=	ENSP00000261937.6:n.3807+419C=
ENST00000393347.7:c.3807+419C=	ENSP00000377016.3:n.3807+419C=
ENST00000502603.5:n.507+419C=
ENST00000502649.5:c.3807+419C=	ENSP00000426057.1:n.3807+419C=
ENST00000507059.5:n.4576C=
ENST00000619105.4:c.*2750+419C=	ENSP00000481134.1:n.*2750+419C=
NM_002020.4:c.3807+419C=	NP_002011.2:n.3807+419C=
NM_182925.4:c.3807+419C=	NP_891555.2:n.3807+419C=
XM_011534477.1:c.4056+419C=	XP_011532779.1:n.4056+419C=
XM_011534478.1:c.4038+419C=	XP_011532780.1:n.4038+419C=
XM_011534479.1:c.4057-255C=	XP_011532781.1:n.4057-255C=
XM_011534480.1:c.4057-255C=	XP_011532782.1:n.4057-255C=
XM_011534481.1:c.4056+419C=	XP_011532783.1:n.4056+419C=
XM_011534482.1:c.3825+419C=	XP_011532784.1:n.3825+419C=
XM_011534483.1:c.3747+419C=	XP_011532785.1:n.3747+419C=
XM_011534484.1:c.3348+419C=	XP_011532786.1:n.3348+419C=
XR_941095.1:n.4093+419C=
NM_001354989.1:c.3807+419C=	NP_001341918.1:n.3807+419C=
XM_011534478.3:c.4038+419C=	XP_011532780.1:n.4038+419C=
XM_011534484.2:c.3348+419C=	XP_011532786.1:n.3348+419C=
XM_017009263.1:c.4039-255C=	XP_016864752.1:n.4039-255C=
XM_017009264.2:c.4039-255C=	XP_016864753.1:n.4039-255C=
XM_017009265.1:c.4039-255C=	XP_016864754.1:n.4039-255C=
XM_017009266.1:c.4038+419C=	XP_016864755.1:n.4038+419C=
XM_017009267.2:c.4038+419C=	XP_016864756.1:n.4038+419C=
XM_017009268.1:c.3729+419C=	XP_016864757.1:n.3729+419C=
XR_001742050.2:n.4297+419C=
NM_182925.5:c.3807+419C= MANE Select	NP_891555.2:n.3807+419C=
NM_001354989.2:c.3807+419C=	NP_001341918.1:n.3807+419C=
NM_002020.5:c.3807+419C=	NP_002011.2:n.3807+419C=