Canonical Allele Identifier: CA2676971904

Gene: FLT4

Linked Data

• gnomAD v4: 5-180614016-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614016G>T , CM000667.2:g.180614016G>T	GRCh38
NC_000005.9:g.180041016G>T , CM000667.1:g.180041016G>T	GRCh37
NC_000005.8:g.179973622G>T	NCBI36
NG_011536.1:g.40609C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3331+52C>A MANE Select	ENSP00000261937.6:n.3331+52C>A
ENST00000261937.10:c.3331+52C>A	ENSP00000261937.6:n.3331+52C>A
ENST00000393347.7:c.3331+52C>A	ENSP00000377016.3:n.3331+52C>A
ENST00000502649.5:c.3331+52C>A	ENSP00000426057.1:n.3331+52C>A
ENST00000507059.5:n.2776C>A
ENST00000619105.4:c.*2274+52C>A	ENSP00000481134.1:n.*2274+52C>A
NM_002020.4:c.3331+52C>A	NP_002011.2:n.3331+52C>A
NM_182925.4:c.3331+52C>A	NP_891555.2:n.3331+52C>A
XM_011534477.1:c.3580+52C>A	XP_011532779.1:n.3580+52C>A
XM_011534478.1:c.3562+52C>A	XP_011532780.1:n.3562+52C>A
XM_011534479.1:c.3580+52C>A	XP_011532781.1:n.3580+52C>A
XM_011534480.1:c.3580+52C>A	XP_011532782.1:n.3580+52C>A
XM_011534481.1:c.3580+52C>A	XP_011532783.1:n.3580+52C>A
XM_011534482.1:c.3349+52C>A	XP_011532784.1:n.3349+52C>A
XM_011534483.1:c.3271+52C>A	XP_011532785.1:n.3271+52C>A
XM_011534484.1:c.2872+52C>A	XP_011532786.1:n.2872+52C>A
XR_941095.1:n.3592+52C>A
NM_001354989.1:c.3331+52C>A	NP_001341918.1:n.3331+52C>A
XM_011534478.3:c.3562+52C>A	XP_011532780.1:n.3562+52C>A
XM_011534484.2:c.2872+52C>A	XP_011532786.1:n.2872+52C>A
XM_017009263.1:c.3562+52C>A	XP_016864752.1:n.3562+52C>A
XM_017009264.2:c.3562+52C>A	XP_016864753.1:n.3562+52C>A
XM_017009265.1:c.3562+52C>A	XP_016864754.1:n.3562+52C>A
XM_017009266.1:c.3562+52C>A	XP_016864755.1:n.3562+52C>A
XM_017009267.2:c.3562+52C>A	XP_016864756.1:n.3562+52C>A
XM_017009268.1:c.3253+52C>A	XP_016864757.1:n.3253+52C>A
XR_001742050.2:n.3796+52C>A
NM_182925.5:c.3331+52C>A MANE Select	NP_891555.2:n.3331+52C>A
NM_001354989.2:c.3331+52C>A	NP_001341918.1:n.3331+52C>A
NM_002020.5:c.3331+52C>A	NP_002011.2:n.3331+52C>A