Canonical Allele Identifier: CA2676968867

Gene: FLT4

Linked Data

• gnomAD v4: 5-180609908-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609908_180609909insT , CM000667.2:g.180609908_180609909insT	GRCh38
NC_000005.9:g.180036908_180036909insT , CM000667.1:g.180036908_180036909insT	GRCh37
NC_000005.8:g.179969514_179969515insT	NCBI36
NG_011536.1:g.44716_44717insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3803_3804insA MANE Select	ENSP00000261937.6:p.Val1269CysfsTer17
ENST00000261937.10:c.3803_3804insA	ENSP00000261937.6:p.Val1269CysfsTer17
ENST00000393347.7:c.3803_3804insA	ENSP00000377016.3:p.Val1269CysfsTer17
ENST00000502603.5:n.503_504insA
ENST00000502649.5:c.3803_3804insA	ENSP00000426057.1:p.Val1269CysfsTer17
ENST00000507059.5:n.4153_4154insA
ENST00000619105.4:c.*2746_*2747insA	ENSP00000481134.1:n.*2746_*2747insA
NM_002020.4:c.3803_3804insA	NP_002011.2:p.Val1269CysfsTer17
NM_182925.4:c.3803_3804insA	NP_891555.2:p.Val1269CysfsTer17
XM_011534477.1:c.4052_4053insA	XP_011532779.1:p.Val1352CysfsTer17
XM_011534478.1:c.4034_4035insA	XP_011532780.1:p.Val1346CysfsTer17
XM_011534479.1:c.4052_4053insA	XP_011532781.1:p.Val1352CysfsTer?
XM_011534480.1:c.4052_4053insA	XP_011532782.1:p.Val1352CysfsTer?
XM_011534481.1:c.4052_4053insA	XP_011532783.1:p.Val1352CysfsTer17
XM_011534482.1:c.3821_3822insA	XP_011532784.1:p.Val1275CysfsTer17
XM_011534483.1:c.3743_3744insA	XP_011532785.1:p.Val1249CysfsTer17
XM_011534484.1:c.3344_3345insA	XP_011532786.1:p.Val1116CysfsTer17
XR_941095.1:n.4089_4090insA
NM_001354989.1:c.3803_3804insA	NP_001341918.1:p.Val1269CysfsTer17
XM_011534478.3:c.4034_4035insA	XP_011532780.1:p.Val1346CysfsTer17
XM_011534484.2:c.3344_3345insA	XP_011532786.1:p.Val1116CysfsTer17
XM_017009263.1:c.4034_4035insA	XP_016864752.1:p.Val1346CysfsTer?
XM_017009264.2:c.4034_4035insA	XP_016864753.1:p.Val1346CysfsTer?
XM_017009265.1:c.4034_4035insA	XP_016864754.1:p.Val1346CysfsTer?
XM_017009266.1:c.4034_4035insA	XP_016864755.1:p.Val1346CysfsTer17
XM_017009267.2:c.4034_4035insA	XP_016864756.1:p.Val1346CysfsTer17
XM_017009268.1:c.3725_3726insA	XP_016864757.1:p.Val1243CysfsTer17
XR_001742050.2:n.4293_4294insA
NM_182925.5:c.3803_3804insA MANE Select	NP_891555.2:p.Val1269CysfsTer17
NM_001354989.2:c.3803_3804insA	NP_001341918.1:p.Val1269CysfsTer17
NM_002020.5:c.3803_3804insA	NP_002011.2:p.Val1269CysfsTer17