Canonical Allele Identifier: CA257464

Gene: FLT4

Linked Data

• ClinVar Variation Id: 16259
• ClinVar RCV Id: RCV000017647 ; RCV003441720
• dbSNP Id: rs267606818
• MyVariant Identifiers: chr5:g.180046743C>T (hg19) ; chr5:g.180619743C>T (hg38)
• PubMed: PMID:10835628

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619743C>T , CM000667.2:g.180619743C>T	GRCh38
NC_000005.9:g.180046743C>T , CM000667.1:g.180046743C>T	GRCh37
NC_000005.8:g.179979349C>T	NCBI36
NG_011536.1:g.34882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2569G>A MANE Select	ENSP00000261937.6:p.Gly857Arg
ENST00000261937.10:c.2569G>A	ENSP00000261937.6:p.Gly857Arg
ENST00000393347.7:c.2569G>A	ENSP00000377016.3:p.Gly857Arg
ENST00000502649.5:c.2569G>A	ENSP00000426057.1:p.Gly857Arg
ENST00000507059.5:n.1664G>A
ENST00000619105.4:c.*1512G>A	ENSP00000481134.1:n.*1512G>A
NM_002020.4:c.2569G>A	NP_002011.2:p.Gly857Arg
NM_182925.4:c.2569G>A	NP_891555.2:p.Gly857Arg
XM_011534477.1:c.2818G>A	XP_011532779.1:p.Gly940Arg
XM_011534478.1:c.2800G>A	XP_011532780.1:p.Gly934Arg
XM_011534479.1:c.2818G>A	XP_011532781.1:p.Gly940Arg
XM_011534480.1:c.2818G>A	XP_011532782.1:p.Gly940Arg
XM_011534481.1:c.2818G>A	XP_011532783.1:p.Gly940Arg
XM_011534482.1:c.2587G>A	XP_011532784.1:p.Gly863Arg
XM_011534483.1:c.2509G>A	XP_011532785.1:p.Gly837Arg
XM_011534484.1:c.2110G>A	XP_011532786.1:p.Gly704Arg
XR_941095.1:n.2830G>A
NM_001354989.1:c.2569G>A	NP_001341918.1:p.Gly857Arg
XM_011534478.3:c.2800G>A	XP_011532780.1:p.Gly934Arg
XM_011534484.2:c.2110G>A	XP_011532786.1:p.Gly704Arg
XM_017009263.1:c.2800G>A	XP_016864752.1:p.Gly934Arg
XM_017009264.2:c.2800G>A	XP_016864753.1:p.Gly934Arg
XM_017009265.1:c.2800G>A	XP_016864754.1:p.Gly934Arg
XM_017009266.1:c.2800G>A	XP_016864755.1:p.Gly934Arg
XM_017009267.2:c.2800G>A	XP_016864756.1:p.Gly934Arg
XM_017009268.1:c.2491G>A	XP_016864757.1:p.Gly831Arg
XR_001742050.2:n.3034G>A
NM_182925.5:c.2569G>A MANE Select	NP_891555.2:p.Gly857Arg
NM_001354989.2:c.2569G>A	NP_001341918.1:p.Gly857Arg
NM_002020.5:c.2569G>A	NP_002011.2:p.Gly857Arg