Canonical Allele Identifier: CA3606181

Gene: FLT4

Linked Data

• dbSNP Id: rs767007351
• ExAC: 5:180046419 C / CGCCACTGG
• MyVariant Identifiers: chr5:g.180046419_180046420insGCCACTGG (hg19) ; chr5:g.180619419_180619420insGCCACTGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180619419_180619420insGCCACTGG , CM000667.2:g.180619419_180619420insGCCACTGG	GRCh38
NC_000005.9:g.180046419_180046420insGCCACTGG , CM000667.1:g.180046419_180046420insGCCACTGG	GRCh37
NC_000005.8:g.179979025_179979026insGCCACTGG	NCBI36
NG_011536.1:g.35205_35206insCCAGTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.2648-54_2648-53insCCAGTGGC MANE Select	ENSP00000261937.6:n.2648-54_2648-53insCCAGTGGC
ENST00000261937.10:c.2648-54_2648-53insCCAGTGGC	ENSP00000261937.6:n.2648-54_2648-53insCCAGTGGC
ENST00000393347.7:c.2648-54_2648-53insCCAGTGGC	ENSP00000377016.3:n.2648-54_2648-53insCCAGTGGC
ENST00000502649.5:c.2648-54_2648-53insCCAGTGGC	ENSP00000426057.1:n.2648-54_2648-53insCCAGTGGC
ENST00000507059.5:n.1987_1988insCCAGTGGC
ENST00000619105.4:c.*1591-54_*1591-53insCCAGTGGC	ENSP00000481134.1:n.*1591-54_*1591-53insCCAGTGGC
NM_002020.4:c.2648-54_2648-53insCCAGTGGC	NP_002011.2:n.2648-54_2648-53insCCAGTGGC
NM_182925.4:c.2648-54_2648-53insCCAGTGGC	NP_891555.2:n.2648-54_2648-53insCCAGTGGC
XM_011534477.1:c.2897-54_2897-53insCCAGTGGC	XP_011532779.1:n.2897-54_2897-53insCCAGTGGC
XM_011534478.1:c.2879-54_2879-53insCCAGTGGC	XP_011532780.1:n.2879-54_2879-53insCCAGTGGC
XM_011534479.1:c.2897-54_2897-53insCCAGTGGC	XP_011532781.1:n.2897-54_2897-53insCCAGTGGC
XM_011534480.1:c.2897-54_2897-53insCCAGTGGC	XP_011532782.1:n.2897-54_2897-53insCCAGTGGC
XM_011534481.1:c.2897-54_2897-53insCCAGTGGC	XP_011532783.1:n.2897-54_2897-53insCCAGTGGC
XM_011534482.1:c.2666-54_2666-53insCCAGTGGC	XP_011532784.1:n.2666-54_2666-53insCCAGTGGC
XM_011534483.1:c.2588-54_2588-53insCCAGTGGC	XP_011532785.1:n.2588-54_2588-53insCCAGTGGC
XM_011534484.1:c.2189-54_2189-53insCCAGTGGC	XP_011532786.1:n.2189-54_2189-53insCCAGTGGC
XR_941095.1:n.2909-54_2909-53insCCAGTGGC
NM_001354989.1:c.2648-54_2648-53insCCAGTGGC	NP_001341918.1:n.2648-54_2648-53insCCAGTGGC
XM_011534478.3:c.2879-54_2879-53insCCAGTGGC	XP_011532780.1:n.2879-54_2879-53insCCAGTGGC
XM_011534484.2:c.2189-54_2189-53insCCAGTGGC	XP_011532786.1:n.2189-54_2189-53insCCAGTGGC
XM_017009263.1:c.2879-54_2879-53insCCAGTGGC	XP_016864752.1:n.2879-54_2879-53insCCAGTGGC
XM_017009264.2:c.2879-54_2879-53insCCAGTGGC	XP_016864753.1:n.2879-54_2879-53insCCAGTGGC
XM_017009265.1:c.2879-54_2879-53insCCAGTGGC	XP_016864754.1:n.2879-54_2879-53insCCAGTGGC
XM_017009266.1:c.2879-54_2879-53insCCAGTGGC	XP_016864755.1:n.2879-54_2879-53insCCAGTGGC
XM_017009267.2:c.2879-54_2879-53insCCAGTGGC	XP_016864756.1:n.2879-54_2879-53insCCAGTGGC
XM_017009268.1:c.2570-54_2570-53insCCAGTGGC	XP_016864757.1:n.2570-54_2570-53insCCAGTGGC
XR_001742050.2:n.3113-54_3113-53insCCAGTGGC
NM_182925.5:c.2648-54_2648-53insCCAGTGGC MANE Select	NP_891555.2:n.2648-54_2648-53insCCAGTGGC
NM_001354989.2:c.2648-54_2648-53insCCAGTGGC	NP_001341918.1:n.2648-54_2648-53insCCAGTGGC
NM_002020.5:c.2648-54_2648-53insCCAGTGGC	NP_002011.2:n.2648-54_2648-53insCCAGTGGC