Canonical Allele Identifier: CA2676972055

Gene: FLT4

Linked Data

• gnomAD v4: 5-180619785-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619786_180619787del , CM000667.2:g.180619786_180619787del	GRCh38
NC_000005.9:g.180046786_180046787del , CM000667.1:g.180046786_180046787del	GRCh37
NC_000005.8:g.179979392_179979393del	NCBI36
NG_011536.1:g.34838_34839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2543-18_2543-17del MANE Select	ENSP00000261937.6:n.2543-18_2543-17del
ENST00000261937.10:c.2543-18_2543-17del	ENSP00000261937.6:n.2543-18_2543-17del
ENST00000393347.7:c.2543-18_2543-17del	ENSP00000377016.3:n.2543-18_2543-17del
ENST00000502649.5:c.2543-18_2543-17del	ENSP00000426057.1:n.2543-18_2543-17del
ENST00000507059.5:n.1638-18_1638-17del
ENST00000619105.4:c.*1486-18_*1486-17del	ENSP00000481134.1:n.*1486-18_*1486-17del
NM_002020.4:c.2543-18_2543-17del	NP_002011.2:n.2543-18_2543-17del
NM_182925.4:c.2543-18_2543-17del	NP_891555.2:n.2543-18_2543-17del
XM_011534477.1:c.2792-18_2792-17del	XP_011532779.1:n.2792-18_2792-17del
XM_011534478.1:c.2774-18_2774-17del	XP_011532780.1:n.2774-18_2774-17del
XM_011534479.1:c.2792-18_2792-17del	XP_011532781.1:n.2792-18_2792-17del
XM_011534480.1:c.2792-18_2792-17del	XP_011532782.1:n.2792-18_2792-17del
XM_011534481.1:c.2792-18_2792-17del	XP_011532783.1:n.2792-18_2792-17del
XM_011534482.1:c.2561-18_2561-17del	XP_011532784.1:n.2561-18_2561-17del
XM_011534483.1:c.2483-18_2483-17del	XP_011532785.1:n.2483-18_2483-17del
XM_011534484.1:c.2084-18_2084-17del	XP_011532786.1:n.2084-18_2084-17del
XR_941095.1:n.2804-18_2804-17del
NM_001354989.1:c.2543-18_2543-17del	NP_001341918.1:n.2543-18_2543-17del
XM_011534478.3:c.2774-18_2774-17del	XP_011532780.1:n.2774-18_2774-17del
XM_011534484.2:c.2084-18_2084-17del	XP_011532786.1:n.2084-18_2084-17del
XM_017009263.1:c.2774-18_2774-17del	XP_016864752.1:n.2774-18_2774-17del
XM_017009264.2:c.2774-18_2774-17del	XP_016864753.1:n.2774-18_2774-17del
XM_017009265.1:c.2774-18_2774-17del	XP_016864754.1:n.2774-18_2774-17del
XM_017009266.1:c.2774-18_2774-17del	XP_016864755.1:n.2774-18_2774-17del
XM_017009267.2:c.2774-18_2774-17del	XP_016864756.1:n.2774-18_2774-17del
XM_017009268.1:c.2465-18_2465-17del	XP_016864757.1:n.2465-18_2465-17del
XR_001742050.2:n.3008-18_3008-17del
NM_182925.5:c.2543-18_2543-17del MANE Select	NP_891555.2:n.2543-18_2543-17del
NM_001354989.2:c.2543-18_2543-17del	NP_001341918.1:n.2543-18_2543-17del
NM_002020.5:c.2543-18_2543-17del	NP_002011.2:n.2543-18_2543-17del