Canonical Allele Identifier: CA1604723162

Gene: FLT4

Linked Data

• dbSNP Id: rs1762988523
• gnomAD v4: 5-180619857-CAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619862_180619864del , CM000667.2:g.180619862_180619864del	GRCh38
NC_000005.9:g.180046862_180046864del , CM000667.1:g.180046862_180046864del	GRCh37
NC_000005.8:g.179979468_179979470del	NCBI36
NG_011536.1:g.34765_34767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2543-91_2543-89del MANE Select	ENSP00000261937.6:n.2543-91_2543-89del
ENST00000261937.10:c.2543-91_2543-89del	ENSP00000261937.6:n.2543-91_2543-89del
ENST00000393347.7:c.2543-91_2543-89del	ENSP00000377016.3:n.2543-91_2543-89del
ENST00000502649.5:c.2543-91_2543-89del	ENSP00000426057.1:n.2543-91_2543-89del
ENST00000507059.5:n.1638-91_1638-89del
ENST00000619105.4:c.*1486-91_*1486-89del	ENSP00000481134.1:n.*1486-91_*1486-89del
NM_002020.4:c.2543-91_2543-89del	NP_002011.2:n.2543-91_2543-89del
NM_182925.4:c.2543-91_2543-89del	NP_891555.2:n.2543-91_2543-89del
XM_011534477.1:c.2792-91_2792-89del	XP_011532779.1:n.2792-91_2792-89del
XM_011534478.1:c.2774-91_2774-89del	XP_011532780.1:n.2774-91_2774-89del
XM_011534479.1:c.2792-91_2792-89del	XP_011532781.1:n.2792-91_2792-89del
XM_011534480.1:c.2792-91_2792-89del	XP_011532782.1:n.2792-91_2792-89del
XM_011534481.1:c.2792-91_2792-89del	XP_011532783.1:n.2792-91_2792-89del
XM_011534482.1:c.2561-91_2561-89del	XP_011532784.1:n.2561-91_2561-89del
XM_011534483.1:c.2483-91_2483-89del	XP_011532785.1:n.2483-91_2483-89del
XM_011534484.1:c.2084-91_2084-89del	XP_011532786.1:n.2084-91_2084-89del
XR_941095.1:n.2804-91_2804-89del
NM_001354989.1:c.2543-91_2543-89del	NP_001341918.1:n.2543-91_2543-89del
XM_011534478.3:c.2774-91_2774-89del	XP_011532780.1:n.2774-91_2774-89del
XM_011534484.2:c.2084-91_2084-89del	XP_011532786.1:n.2084-91_2084-89del
XM_017009263.1:c.2774-91_2774-89del	XP_016864752.1:n.2774-91_2774-89del
XM_017009264.2:c.2774-91_2774-89del	XP_016864753.1:n.2774-91_2774-89del
XM_017009265.1:c.2774-91_2774-89del	XP_016864754.1:n.2774-91_2774-89del
XM_017009266.1:c.2774-91_2774-89del	XP_016864755.1:n.2774-91_2774-89del
XM_017009267.2:c.2774-91_2774-89del	XP_016864756.1:n.2774-91_2774-89del
XM_017009268.1:c.2465-91_2465-89del	XP_016864757.1:n.2465-91_2465-89del
XR_001742050.2:n.3008-91_3008-89del
NM_182925.5:c.2543-91_2543-89del MANE Select	NP_891555.2:n.2543-91_2543-89del
NM_001354989.2:c.2543-91_2543-89del	NP_001341918.1:n.2543-91_2543-89del
NM_002020.5:c.2543-91_2543-89del	NP_002011.2:n.2543-91_2543-89del