Canonical Allele Identifier: CA1604719152

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180613055T= , CM000667.2:g.180613055T=	GRCh38
NC_000005.9:g.180040055T= , CM000667.1:g.180040055T=	GRCh37
NC_000005.8:g.179972661T=	NCBI36
NG_011536.1:g.41570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3387A= MANE Select	ENSP00000261937.6:p.Arg1129=
ENST00000261937.10:c.3387A=	ENSP00000261937.6:p.Arg1129=
ENST00000393347.7:c.3387A=	ENSP00000377016.3:p.Arg1129=
ENST00000502649.5:c.3387A=	ENSP00000426057.1:p.Arg1129=
ENST00000507059.5:n.3737A=
ENST00000510000.1:n.339A=
ENST00000619105.4:c.*2330A=	ENSP00000481134.1:n.*2330A=
NM_002020.4:c.3387A=	NP_002011.2:p.Arg1129=
NM_182925.4:c.3387A=	NP_891555.2:p.Arg1129=
XM_011534477.1:c.3636A=	XP_011532779.1:p.Arg1212=
XM_011534478.1:c.3618A=	XP_011532780.1:p.Arg1206=
XM_011534479.1:c.3636A=	XP_011532781.1:p.Arg1212=
XM_011534480.1:c.3636A=	XP_011532782.1:p.Arg1212=
XM_011534481.1:c.3636A=	XP_011532783.1:p.Arg1212=
XM_011534482.1:c.3405A=	XP_011532784.1:p.Arg1135=
XM_011534483.1:c.3327A=	XP_011532785.1:p.Arg1109=
XM_011534484.1:c.2928A=	XP_011532786.1:p.Arg976=
XR_941095.1:n.3648A=
NM_001354989.1:c.3387A=	NP_001341918.1:p.Arg1129=
XM_011534478.3:c.3618A=	XP_011532780.1:p.Arg1206=
XM_011534484.2:c.2928A=	XP_011532786.1:p.Arg976=
XM_017009263.1:c.3618A=	XP_016864752.1:p.Arg1206=
XM_017009264.2:c.3618A=	XP_016864753.1:p.Arg1206=
XM_017009265.1:c.3618A=	XP_016864754.1:p.Arg1206=
XM_017009266.1:c.3618A=	XP_016864755.1:p.Arg1206=
XM_017009267.2:c.3618A=	XP_016864756.1:p.Arg1206=
XM_017009268.1:c.3309A=	XP_016864757.1:p.Arg1103=
XR_001742050.2:n.3852A=
NM_182925.5:c.3387A= MANE Select	NP_891555.2:p.Arg1129=
NM_001354989.2:c.3387A=	NP_001341918.1:p.Arg1129=
NM_002020.5:c.3387A=	NP_002011.2:p.Arg1129=