Canonical Allele Identifier: CA362501605

Gene: FLT4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619344G>T , CM000667.2:g.180619344G>T	GRCh38
NC_000005.9:g.180046344G>T , CM000667.1:g.180046344G>T	GRCh37
NC_000005.8:g.179978950G>T	NCBI36
NG_011536.1:g.35281C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2670C>A MANE Select	ENSP00000261937.6:p.His890Gln
ENST00000261937.10:c.2670C>A	ENSP00000261937.6:p.His890Gln
ENST00000393347.7:c.2670C>A	ENSP00000377016.3:p.His890Gln
ENST00000502649.5:c.2670C>A	ENSP00000426057.1:p.His890Gln
ENST00000507059.5:n.2063C>A
ENST00000512795.1:c.-128C>A	ENSP00000421535.1:n.-128C>A
ENST00000619105.4:c.*1613C>A	ENSP00000481134.1:n.*1613C>A
NM_002020.4:c.2670C>A	NP_002011.2:p.His890Gln
NM_182925.4:c.2670C>A	NP_891555.2:p.His890Gln
XM_011534477.1:c.2919C>A	XP_011532779.1:p.His973Gln
XM_011534478.1:c.2901C>A	XP_011532780.1:p.His967Gln
XM_011534479.1:c.2919C>A	XP_011532781.1:p.His973Gln
XM_011534480.1:c.2919C>A	XP_011532782.1:p.His973Gln
XM_011534481.1:c.2919C>A	XP_011532783.1:p.His973Gln
XM_011534482.1:c.2688C>A	XP_011532784.1:p.His896Gln
XM_011534483.1:c.2610C>A	XP_011532785.1:p.His870Gln
XM_011534484.1:c.2211C>A	XP_011532786.1:p.His737Gln
XR_941095.1:n.2931C>A
NM_001354989.1:c.2670C>A	NP_001341918.1:p.His890Gln
XM_011534478.3:c.2901C>A	XP_011532780.1:p.His967Gln
XM_011534484.2:c.2211C>A	XP_011532786.1:p.His737Gln
XM_017009263.1:c.2901C>A	XP_016864752.1:p.His967Gln
XM_017009264.2:c.2901C>A	XP_016864753.1:p.His967Gln
XM_017009265.1:c.2901C>A	XP_016864754.1:p.His967Gln
XM_017009266.1:c.2901C>A	XP_016864755.1:p.His967Gln
XM_017009267.2:c.2901C>A	XP_016864756.1:p.His967Gln
XM_017009268.1:c.2592C>A	XP_016864757.1:p.His864Gln
XR_001742050.2:n.3135C>A
NM_182925.5:c.2670C>A MANE Select	NP_891555.2:p.His890Gln
NM_001354989.2:c.2670C>A	NP_001341918.1:p.His890Gln
NM_002020.5:c.2670C>A	NP_002011.2:p.His890Gln