Canonical Allele Identifier: CA1604722565

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180618911G= , CM000667.2:g.180618911G=	GRCh38
NC_000005.9:g.180045911G= , CM000667.1:g.180045911G=	GRCh37
NC_000005.8:g.179978517G=	NCBI36
NG_011536.1:g.35714C=

Transcript Alleles

HGVS	Amino-acid Change
NM_182925.5:c.2860C= MANE Select	NP_891555.2:p.Pro954=
ENST00000261937.11:c.2860C= MANE Select	ENSP00000261937.6:p.Pro954=
NM_001354989.1:c.2860C=	NP_001341918.1:p.Pro954=
NM_001354989.2:c.2860C=	NP_001341918.1:p.Pro954=
NM_002020.4:c.2860C=	NP_002011.2:p.Pro954=
NM_002020.5:c.2860C=	NP_002011.2:p.Pro954=
NM_182925.4:c.2860C=	NP_891555.2:p.Pro954=
ENST00000261937.10:c.2860C=	ENSP00000261937.6:p.Pro954=
ENST00000393347.7:c.2860C=	ENSP00000377016.3:p.Pro954=
ENST00000502649.5:c.2860C=	ENSP00000426057.1:p.Pro954=
ENST00000507059.5:n.2253C=
ENST00000512795.1:c.-27C=	ENSP00000421535.1:n.-27C=
ENST00000514810.1:n.227C=
ENST00000619105.4:c.*1803C=	ENSP00000481134.1:n.*1803C=
XM_011534477.1:c.3109C=	XP_011532779.1:p.Pro1037=
XM_011534478.1:c.3091C=	XP_011532780.1:p.Pro1031=
XM_011534478.3:c.3091C=	XP_011532780.1:p.Pro1031=
XM_011534479.1:c.3109C=	XP_011532781.1:p.Pro1037=
XM_011534480.1:c.3109C=	XP_011532782.1:p.Pro1037=
XM_011534481.1:c.3109C=	XP_011532783.1:p.Pro1037=
XM_011534482.1:c.2878C=	XP_011532784.1:p.Pro960=
XM_011534483.1:c.2800C=	XP_011532785.1:p.Pro934=
XM_011534484.1:c.2401C=	XP_011532786.1:p.Pro801=
XM_011534484.2:c.2401C=	XP_011532786.1:p.Pro801=
XM_017009263.1:c.3091C=	XP_016864752.1:p.Pro1031=
XM_017009264.2:c.3091C=	XP_016864753.1:p.Pro1031=
XM_017009265.1:c.3091C=	XP_016864754.1:p.Pro1031=
XM_017009266.1:c.3091C=	XP_016864755.1:p.Pro1031=
XM_017009267.2:c.3091C=	XP_016864756.1:p.Pro1031=
XM_017009268.1:c.2782C=	XP_016864757.1:p.Pro928=
XR_001742050.2:n.3325C=
XR_941095.1:n.3121C=