Canonical Allele Identifier: CA1604720335

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614160C= , CM000667.2:g.180614160C=	GRCh38
NC_000005.9:g.180041160C= , CM000667.1:g.180041160C=	GRCh37
NC_000005.8:g.179973766C=	NCBI36
NG_011536.1:g.40465G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3239G= MANE Select	ENSP00000261937.6:p.Trp1080=
ENST00000261937.10:c.3239G=	ENSP00000261937.6:p.Trp1080=
ENST00000393347.7:c.3239G=	ENSP00000377016.3:p.Trp1080=
ENST00000502649.5:c.3239G=	ENSP00000426057.1:p.Trp1080=
ENST00000507059.5:n.2632G=
ENST00000512795.1:c.353G=	ENSP00000421535.1:p.Trp118=
ENST00000514810.1:n.606G=
ENST00000619105.4:c.*2182G=	ENSP00000481134.1:n.*2182G=
NM_002020.4:c.3239G=	NP_002011.2:p.Trp1080=
NM_182925.4:c.3239G=	NP_891555.2:p.Trp1080=
XM_011534477.1:c.3488G=	XP_011532779.1:p.Trp1163=
XM_011534478.1:c.3470G=	XP_011532780.1:p.Trp1157=
XM_011534479.1:c.3488G=	XP_011532781.1:p.Trp1163=
XM_011534480.1:c.3488G=	XP_011532782.1:p.Trp1163=
XM_011534481.1:c.3488G=	XP_011532783.1:p.Trp1163=
XM_011534482.1:c.3257G=	XP_011532784.1:p.Trp1086=
XM_011534483.1:c.3179G=	XP_011532785.1:p.Trp1060=
XM_011534484.1:c.2780G=	XP_011532786.1:p.Trp927=
XR_941095.1:n.3500G=
NM_001354989.1:c.3239G=	NP_001341918.1:p.Trp1080=
XM_011534478.3:c.3470G=	XP_011532780.1:p.Trp1157=
XM_011534484.2:c.2780G=	XP_011532786.1:p.Trp927=
XM_017009263.1:c.3470G=	XP_016864752.1:p.Trp1157=
XM_017009264.2:c.3470G=	XP_016864753.1:p.Trp1157=
XM_017009265.1:c.3470G=	XP_016864754.1:p.Trp1157=
XM_017009266.1:c.3470G=	XP_016864755.1:p.Trp1157=
XM_017009267.2:c.3470G=	XP_016864756.1:p.Trp1157=
XM_017009268.1:c.3161G=	XP_016864757.1:p.Trp1054=
XR_001742050.2:n.3704G=
NM_182925.5:c.3239G= MANE Select	NP_891555.2:p.Trp1080=
NM_001354989.2:c.3239G=	NP_001341918.1:p.Trp1080=
NM_002020.5:c.3239G=	NP_002011.2:p.Trp1080=