Canonical Allele Identifier: CA1604723092

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619753G= , CM000667.2:g.180619753G=	GRCh38
NC_000005.9:g.180046753G= , CM000667.1:g.180046753G=	GRCh37
NC_000005.8:g.179979359G=	NCBI36
NG_011536.1:g.34872C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.2559C= MANE Select	ENSP00000261937.6:p.Tyr853=
ENST00000261937.10:c.2559C=	ENSP00000261937.6:p.Tyr853=
ENST00000393347.7:c.2559C=	ENSP00000377016.3:p.Tyr853=
ENST00000502649.5:c.2559C=	ENSP00000426057.1:p.Tyr853=
ENST00000507059.5:n.1654C=
ENST00000619105.4:c.*1502C=	ENSP00000481134.1:n.*1502C=
NM_002020.4:c.2559C=	NP_002011.2:p.Tyr853=
NM_182925.4:c.2559C=	NP_891555.2:p.Tyr853=
XM_011534477.1:c.2808C=	XP_011532779.1:p.Tyr936=
XM_011534478.1:c.2790C=	XP_011532780.1:p.Tyr930=
XM_011534479.1:c.2808C=	XP_011532781.1:p.Tyr936=
XM_011534480.1:c.2808C=	XP_011532782.1:p.Tyr936=
XM_011534481.1:c.2808C=	XP_011532783.1:p.Tyr936=
XM_011534482.1:c.2577C=	XP_011532784.1:p.Tyr859=
XM_011534483.1:c.2499C=	XP_011532785.1:p.Tyr833=
XM_011534484.1:c.2100C=	XP_011532786.1:p.Tyr700=
XR_941095.1:n.2820C=
NM_001354989.1:c.2559C=	NP_001341918.1:p.Tyr853=
XM_011534478.3:c.2790C=	XP_011532780.1:p.Tyr930=
XM_011534484.2:c.2100C=	XP_011532786.1:p.Tyr700=
XM_017009263.1:c.2790C=	XP_016864752.1:p.Tyr930=
XM_017009264.2:c.2790C=	XP_016864753.1:p.Tyr930=
XM_017009265.1:c.2790C=	XP_016864754.1:p.Tyr930=
XM_017009266.1:c.2790C=	XP_016864755.1:p.Tyr930=
XM_017009267.2:c.2790C=	XP_016864756.1:p.Tyr930=
XM_017009268.1:c.2481C=	XP_016864757.1:p.Tyr827=
XR_001742050.2:n.3024C=
NM_182925.5:c.2559C= MANE Select	NP_891555.2:p.Tyr853=
NM_001354989.2:c.2559C=	NP_001341918.1:p.Tyr853=
NM_002020.5:c.2559C=	NP_002011.2:p.Tyr853=