Canonical Allele Identifier: CA2676971602

Gene: FLT4

Linked Data

• gnomAD v4: 5-180613904-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180613907_180613908del , CM000667.2:g.180613907_180613908del	GRCh38
NC_000005.9:g.180040907_180040908del , CM000667.1:g.180040907_180040908del	GRCh37
NC_000005.8:g.179973513_179973514del	NCBI36
NG_011536.1:g.40719_40720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3331+162_3331+163del MANE Select	ENSP00000261937.6:n.3331+162_3331+163del
ENST00000261937.10:c.3331+162_3331+163del	ENSP00000261937.6:n.3331+162_3331+163del
ENST00000393347.7:c.3331+162_3331+163del	ENSP00000377016.3:n.3331+162_3331+163del
ENST00000502649.5:c.3331+162_3331+163del	ENSP00000426057.1:n.3331+162_3331+163del
ENST00000507059.5:n.2886_2887del
ENST00000619105.4:c.*2274+162_*2274+163del	ENSP00000481134.1:n.*2274+162_*2274+163del
NM_002020.4:c.3331+162_3331+163del	NP_002011.2:n.3331+162_3331+163del
NM_182925.4:c.3331+162_3331+163del	NP_891555.2:n.3331+162_3331+163del
XM_011534477.1:c.3580+162_3580+163del	XP_011532779.1:n.3580+162_3580+163del
XM_011534478.1:c.3562+162_3562+163del	XP_011532780.1:n.3562+162_3562+163del
XM_011534479.1:c.3580+162_3580+163del	XP_011532781.1:n.3580+162_3580+163del
XM_011534480.1:c.3580+162_3580+163del	XP_011532782.1:n.3580+162_3580+163del
XM_011534481.1:c.3580+162_3580+163del	XP_011532783.1:n.3580+162_3580+163del
XM_011534482.1:c.3349+162_3349+163del	XP_011532784.1:n.3349+162_3349+163del
XM_011534483.1:c.3271+162_3271+163del	XP_011532785.1:n.3271+162_3271+163del
XM_011534484.1:c.2872+162_2872+163del	XP_011532786.1:n.2872+162_2872+163del
XR_941095.1:n.3592+162_3592+163del
NM_001354989.1:c.3331+162_3331+163del	NP_001341918.1:n.3331+162_3331+163del
XM_011534478.3:c.3562+162_3562+163del	XP_011532780.1:n.3562+162_3562+163del
XM_011534484.2:c.2872+162_2872+163del	XP_011532786.1:n.2872+162_2872+163del
XM_017009263.1:c.3562+162_3562+163del	XP_016864752.1:n.3562+162_3562+163del
XM_017009264.2:c.3562+162_3562+163del	XP_016864753.1:n.3562+162_3562+163del
XM_017009265.1:c.3562+162_3562+163del	XP_016864754.1:n.3562+162_3562+163del
XM_017009266.1:c.3562+162_3562+163del	XP_016864755.1:n.3562+162_3562+163del
XM_017009267.2:c.3562+162_3562+163del	XP_016864756.1:n.3562+162_3562+163del
XM_017009268.1:c.3253+162_3253+163del	XP_016864757.1:n.3253+162_3253+163del
XR_001742050.2:n.3796+162_3796+163del
NM_182925.5:c.3331+162_3331+163del MANE Select	NP_891555.2:n.3331+162_3331+163del
NM_001354989.2:c.3331+162_3331+163del	NP_001341918.1:n.3331+162_3331+163del
NM_002020.5:c.3331+162_3331+163del	NP_002011.2:n.3331+162_3331+163del