Canonical Allele Identifier: CA564958478

Gene: FLT4

Linked Data

• dbSNP Id: rs773431033
• gnomAD v2: 5-180030319-G-GGCCGCC
• gnomAD v4: 5-180603319-G-GGCCGCC
• MyVariant Identifiers: chr5:g.180030322_180030323insGCCGCC (hg19) ; chr5:g.180603322_180603323insGCCGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603326_180603331dup , CM000667.2:g.180603326_180603331dup	GRCh38
NC_000005.9:g.180030326_180030331dup , CM000667.1:g.180030326_180030331dup	GRCh37
NC_000005.8:g.179962932_179962937dup	NCBI36
NG_011536.1:g.51300_51305dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3959_3964dup MANE Select	ENSP00000261937.6:p.Arg1321_Pro1322insArgArg
ENST00000261937.10:c.3959_3964dup	ENSP00000261937.6:p.Arg1321_Pro1322insArgArg
ENST00000502603.5:n.659_664dup
NM_182925.4:c.3959_3964dup	NP_891555.2:p.Arg1321_Pro1322insArgArg
XM_011534477.1:c.4208_4213dup	XP_011532779.1:p.Arg1404_Pro1405insArgArg
XM_011534478.1:c.4190_4195dup	XP_011532780.1:p.Arg1398_Pro1399insArgArg
XM_011534479.1:c.*105_*110dup	XP_011532781.1:n.*105_*110dup
XM_011534482.1:c.3977_3982dup	XP_011532784.1:p.Arg1327_Pro1328insArgArg
XM_011534483.1:c.3899_3904dup	XP_011532785.1:p.Arg1301_Pro1302insArgArg
XM_011534484.1:c.3500_3505dup	XP_011532786.1:p.Arg1168_Pro1169insArgArg
XR_941095.1:n.4245_4250dup
XM_011534478.3:c.4190_4195dup	XP_011532780.1:p.Arg1398_Pro1399insArgArg
XM_011534484.2:c.3500_3505dup	XP_011532786.1:p.Arg1168_Pro1169insArgArg
XM_017009263.1:c.*105_*110dup	XP_016864752.1:n.*105_*110dup
XM_017009268.1:c.3881_3886dup	XP_016864757.1:p.Arg1295_Pro1296insArgArg
XR_001742050.2:n.4449_4454dup
NM_182925.5:c.3959_3964dup MANE Select	NP_891555.2:p.Arg1321_Pro1322insArgArg