Canonical Allele Identifier: CA3605615

Gene: FLT4

Linked Data

• dbSNP Id: rs773431033
• ExAC: 5:180030319 GGCC / G
• gnomAD v2: 5-180030319-GGCC-G
• gnomAD v3: 5-180603319-GGCC-G
• gnomAD v4: 5-180603319-GGCC-G
• MyVariant Identifiers: chr5:g.180030320_180030322del (hg19) ; chr5:g.180603320_180603322del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603329_180603331del , CM000667.2:g.180603329_180603331del	GRCh38
NC_000005.9:g.180030329_180030331del , CM000667.1:g.180030329_180030331del	GRCh37
NC_000005.8:g.179962935_179962937del	NCBI36
NG_011536.1:g.51303_51305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3962_3964del MANE Select	ENSP00000261937.6:p.Arg1321del
ENST00000261937.10:c.3962_3964del	ENSP00000261937.6:p.Arg1321del
ENST00000502603.5:n.662_664del
NM_182925.4:c.3962_3964del	NP_891555.2:p.Arg1321del
XM_011534477.1:c.4211_4213del	XP_011532779.1:p.Arg1404del
XM_011534478.1:c.4193_4195del	XP_011532780.1:p.Arg1398del
XM_011534479.1:c.*108_*110del	XP_011532781.1:n.*108_*110del
XM_011534482.1:c.3980_3982del	XP_011532784.1:p.Arg1327del
XM_011534483.1:c.3902_3904del	XP_011532785.1:p.Arg1301del
XM_011534484.1:c.3503_3505del	XP_011532786.1:p.Arg1168del
XR_941095.1:n.4248_4250del
XM_011534478.3:c.4193_4195del	XP_011532780.1:p.Arg1398del
XM_011534484.2:c.3503_3505del	XP_011532786.1:p.Arg1168del
XM_017009263.1:c.*108_*110del	XP_016864752.1:n.*108_*110del
XM_017009268.1:c.3884_3886del	XP_016864757.1:p.Arg1295del
XR_001742050.2:n.4452_4454del
NM_182925.5:c.3962_3964del MANE Select	NP_891555.2:p.Arg1321del