Canonical Allele Identifier: CA2676966978

Gene: FLT4

Linked Data

• gnomAD v4: 5-180602490-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602490G>T , CM000667.2:g.180602490G>T	GRCh38
NC_000005.9:g.180029490G>T , CM000667.1:g.180029490G>T	GRCh37
NC_000005.8:g.179962096G>T	NCBI36
NG_011536.1:g.52135C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*702C>A MANE Select	ENSP00000261937.6:n.*702C>A
ENST00000261937.10:c.*702C>A	ENSP00000261937.6:n.*702C>A
NM_182925.4:c.*702C>A	NP_891555.2:n.*702C>A
XM_011534477.1:c.*702C>A	XP_011532779.1:n.*702C>A
XM_011534478.1:c.*702C>A	XP_011532780.1:n.*702C>A
XM_011534482.1:c.*702C>A	XP_011532784.1:n.*702C>A
XM_011534483.1:c.*702C>A	XP_011532785.1:n.*702C>A
XM_011534484.1:c.*702C>A	XP_011532786.1:n.*702C>A
XM_011534478.3:c.*702C>A	XP_011532780.1:n.*702C>A
XM_011534484.2:c.*702C>A	XP_011532786.1:n.*702C>A
XM_017009263.1:c.*940C>A	XP_016864752.1:n.*940C>A
XM_017009268.1:c.*702C>A	XP_016864757.1:n.*702C>A
XR_001742050.2:n.5284C>A
NM_182925.5:c.*702C>A MANE Select	NP_891555.2:n.*702C>A