Canonical Allele Identifier: CA3605622

Gene: FLT4

Linked Data

• dbSNP Id: rs145806915
• ExAC: 5:180030328 C / T
• gnomAD v2: 5-180030328-C-T
• gnomAD v3: 5-180603328-C-T
• gnomAD v4: 5-180603328-C-T
• MyVariant Identifiers: chr5:g.180030328C>T (hg19) ; chr5:g.180603328C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603328C>T , CM000667.2:g.180603328C>T	GRCh38
NC_000005.9:g.180030328C>T , CM000667.1:g.180030328C>T	GRCh37
NC_000005.8:g.179962934C>T	NCBI36
NG_011536.1:g.51297G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3956G>A MANE Select	ENSP00000261937.6:p.Arg1319Gln
ENST00000261937.10:c.3956G>A	ENSP00000261937.6:p.Arg1319Gln
ENST00000502603.5:n.656G>A
NM_182925.4:c.3956G>A	NP_891555.2:p.Arg1319Gln
XM_011534477.1:c.4205G>A	XP_011532779.1:p.Arg1402Gln
XM_011534478.1:c.4187G>A	XP_011532780.1:p.Arg1396Gln
XM_011534479.1:c.*102G>A	XP_011532781.1:n.*102G>A
XM_011534482.1:c.3974G>A	XP_011532784.1:p.Arg1325Gln
XM_011534483.1:c.3896G>A	XP_011532785.1:p.Arg1299Gln
XM_011534484.1:c.3497G>A	XP_011532786.1:p.Arg1166Gln
XR_941095.1:n.4242G>A
XM_011534478.3:c.4187G>A	XP_011532780.1:p.Arg1396Gln
XM_011534484.2:c.3497G>A	XP_011532786.1:p.Arg1166Gln
XM_017009263.1:c.*102G>A	XP_016864752.1:n.*102G>A
XM_017009268.1:c.3878G>A	XP_016864757.1:p.Arg1293Gln
XR_001742050.2:n.4446G>A
NM_182925.5:c.3956G>A MANE Select	NP_891555.2:p.Arg1319Gln