Canonical Allele Identifier: CA2518376942

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180613902_180613903insA , CM000667.2:g.180613902_180613903insA	GRCh38
NC_000005.9:g.180040902_180040903insA , CM000667.1:g.180040902_180040903insA	GRCh37
NC_000005.8:g.179973508_179973509insA	NCBI36
NG_011536.1:g.40722_40723insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3331+165_3331+166insT MANE Select	ENSP00000261937.6:n.3331+165_3331+166insT
ENST00000261937.10:c.3331+165_3331+166insT	ENSP00000261937.6:n.3331+165_3331+166insT
ENST00000393347.7:c.3331+165_3331+166insT	ENSP00000377016.3:n.3331+165_3331+166insT
ENST00000502649.5:c.3331+165_3331+166insT	ENSP00000426057.1:n.3331+165_3331+166insT
ENST00000507059.5:n.2889_2890insT
ENST00000619105.4:c.*2274+165_*2274+166insT	ENSP00000481134.1:n.*2274+165_*2274+166insT
NM_002020.4:c.3331+165_3331+166insT	NP_002011.2:n.3331+165_3331+166insT
NM_182925.4:c.3331+165_3331+166insT	NP_891555.2:n.3331+165_3331+166insT
XM_011534477.1:c.3580+165_3580+166insT	XP_011532779.1:n.3580+165_3580+166insT
XM_011534478.1:c.3562+165_3562+166insT	XP_011532780.1:n.3562+165_3562+166insT
XM_011534479.1:c.3580+165_3580+166insT	XP_011532781.1:n.3580+165_3580+166insT
XM_011534480.1:c.3580+165_3580+166insT	XP_011532782.1:n.3580+165_3580+166insT
XM_011534481.1:c.3580+165_3580+166insT	XP_011532783.1:n.3580+165_3580+166insT
XM_011534482.1:c.3349+165_3349+166insT	XP_011532784.1:n.3349+165_3349+166insT
XM_011534483.1:c.3271+165_3271+166insT	XP_011532785.1:n.3271+165_3271+166insT
XM_011534484.1:c.2872+165_2872+166insT	XP_011532786.1:n.2872+165_2872+166insT
XR_941095.1:n.3592+165_3592+166insT
NM_001354989.1:c.3331+165_3331+166insT	NP_001341918.1:n.3331+165_3331+166insT
XM_011534478.3:c.3562+165_3562+166insT	XP_011532780.1:n.3562+165_3562+166insT
XM_011534484.2:c.2872+165_2872+166insT	XP_011532786.1:n.2872+165_2872+166insT
XM_017009263.1:c.3562+165_3562+166insT	XP_016864752.1:n.3562+165_3562+166insT
XM_017009264.2:c.3562+165_3562+166insT	XP_016864753.1:n.3562+165_3562+166insT
XM_017009265.1:c.3562+165_3562+166insT	XP_016864754.1:n.3562+165_3562+166insT
XM_017009266.1:c.3562+165_3562+166insT	XP_016864755.1:n.3562+165_3562+166insT
XM_017009267.2:c.3562+165_3562+166insT	XP_016864756.1:n.3562+165_3562+166insT
XM_017009268.1:c.3253+165_3253+166insT	XP_016864757.1:n.3253+165_3253+166insT
XR_001742050.2:n.3796+165_3796+166insT
NM_182925.5:c.3331+165_3331+166insT MANE Select	NP_891555.2:n.3331+165_3331+166insT
NM_001354989.2:c.3331+165_3331+166insT	NP_001341918.1:n.3331+165_3331+166insT
NM_002020.5:c.3331+165_3331+166insT	NP_002011.2:n.3331+165_3331+166insT