Canonical Allele Identifier: CA3606153

Gene: FLT4

Linked Data

• ClinVar Variation Id: 263039
• ClinVar RCV Id: RCV000251871 ; RCV001660381 ; RCV001701830 ; RCV001701923
• dbSNP Id: rs448012
• ExAC: 5:180046344 G / C
• gnomAD v2: 5-180046344-G-C
• gnomAD v3: 5-180619344-G-C
• gnomAD v4: 5-180619344-G-C
• MyVariant Identifiers: chr5:g.180046344G>C (hg19) ; chr5:g.180619344G>C (hg38)

Genomic Alleles

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

Transcript Alleles

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