Canonical Allele Identifier: CA362495690

Gene: FLT4

Linked Data

• dbSNP Id: rs1325967047
• gnomAD v3: 5-180603269-C-T
• gnomAD v4: 5-180603269-C-T
• COSMIC: COSM3614868
• MyVariant Identifiers: chr5:g.180030269C>T (hg19) ; chr5:g.180603269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603269C>T , CM000667.2:g.180603269C>T	GRCh38
NC_000005.9:g.180030269C>T , CM000667.1:g.180030269C>T	GRCh37
NC_000005.8:g.179962875C>T	NCBI36
NG_011536.1:g.51356G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4015G>A MANE Select	ENSP00000261937.6:p.Glu1339Lys
ENST00000261937.10:c.4015G>A	ENSP00000261937.6:p.Glu1339Lys
ENST00000502603.5:n.715G>A
NM_182925.4:c.4015G>A	NP_891555.2:p.Glu1339Lys
XM_011534477.1:c.4264G>A	XP_011532779.1:p.Glu1422Lys
XM_011534478.1:c.4246G>A	XP_011532780.1:p.Glu1416Lys
XM_011534482.1:c.4033G>A	XP_011532784.1:p.Glu1345Lys
XM_011534483.1:c.3955G>A	XP_011532785.1:p.Glu1319Lys
XM_011534484.1:c.3556G>A	XP_011532786.1:p.Glu1186Lys
XR_941095.1:n.4301G>A
XM_011534478.3:c.4246G>A	XP_011532780.1:p.Glu1416Lys
XM_011534484.2:c.3556G>A	XP_011532786.1:p.Glu1186Lys
XM_017009263.1:c.*161G>A	XP_016864752.1:n.*161G>A
XM_017009268.1:c.3937G>A	XP_016864757.1:p.Glu1313Lys
XR_001742050.2:n.4505G>A
NM_182925.5:c.4015G>A MANE Select	NP_891555.2:p.Glu1339Lys