Canonical Allele Identifier: CA3606212

Gene: FLT4

Linked Data

• dbSNP Id: rs781512497
• ExAC: 5:180046435 TTTGGG / T
• gnomAD v2: 5-180046435-TTTGGG-T
• gnomAD v4: 5-180619435-TTTGGG-T
• MyVariant Identifiers: chr5:g.180046436_180046440del (hg19) ; chr5:g.180619436_180619440del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619436_180619440del , CM000667.2:g.180619436_180619440del	GRCh38
NC_000005.9:g.180046436_180046440del , CM000667.1:g.180046436_180046440del	GRCh37
NC_000005.8:g.179979042_179979046del	NCBI36
NG_011536.1:g.35185_35189del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-74_2648-70del MANE Select	ENSP00000261937.6:n.2648-74_2648-70del
ENST00000261937.10:c.2648-74_2648-70del	ENSP00000261937.6:n.2648-74_2648-70del
ENST00000393347.7:c.2648-74_2648-70del	ENSP00000377016.3:n.2648-74_2648-70del
ENST00000502649.5:c.2648-74_2648-70del	ENSP00000426057.1:n.2648-74_2648-70del
ENST00000507059.5:n.1967_1971del
ENST00000619105.4:c.*1591-74_*1591-70del	ENSP00000481134.1:n.*1591-74_*1591-70del
NM_002020.4:c.2648-74_2648-70del	NP_002011.2:n.2648-74_2648-70del
NM_182925.4:c.2648-74_2648-70del	NP_891555.2:n.2648-74_2648-70del
XM_011534477.1:c.2897-74_2897-70del	XP_011532779.1:n.2897-74_2897-70del
XM_011534478.1:c.2879-74_2879-70del	XP_011532780.1:n.2879-74_2879-70del
XM_011534479.1:c.2897-74_2897-70del	XP_011532781.1:n.2897-74_2897-70del
XM_011534480.1:c.2897-74_2897-70del	XP_011532782.1:n.2897-74_2897-70del
XM_011534481.1:c.2897-74_2897-70del	XP_011532783.1:n.2897-74_2897-70del
XM_011534482.1:c.2666-74_2666-70del	XP_011532784.1:n.2666-74_2666-70del
XM_011534483.1:c.2588-74_2588-70del	XP_011532785.1:n.2588-74_2588-70del
XM_011534484.1:c.2189-74_2189-70del	XP_011532786.1:n.2189-74_2189-70del
XR_941095.1:n.2909-74_2909-70del
NM_001354989.1:c.2648-74_2648-70del	NP_001341918.1:n.2648-74_2648-70del
XM_011534478.3:c.2879-74_2879-70del	XP_011532780.1:n.2879-74_2879-70del
XM_011534484.2:c.2189-74_2189-70del	XP_011532786.1:n.2189-74_2189-70del
XM_017009263.1:c.2879-74_2879-70del	XP_016864752.1:n.2879-74_2879-70del
XM_017009264.2:c.2879-74_2879-70del	XP_016864753.1:n.2879-74_2879-70del
XM_017009265.1:c.2879-74_2879-70del	XP_016864754.1:n.2879-74_2879-70del
XM_017009266.1:c.2879-74_2879-70del	XP_016864755.1:n.2879-74_2879-70del
XM_017009267.2:c.2879-74_2879-70del	XP_016864756.1:n.2879-74_2879-70del
XM_017009268.1:c.2570-74_2570-70del	XP_016864757.1:n.2570-74_2570-70del
XR_001742050.2:n.3113-74_3113-70del
NM_182925.5:c.2648-74_2648-70del MANE Select	NP_891555.2:n.2648-74_2648-70del
NM_001354989.2:c.2648-74_2648-70del	NP_001341918.1:n.2648-74_2648-70del
NM_002020.5:c.2648-74_2648-70del	NP_002011.2:n.2648-74_2648-70del