Canonical Allele Identifier: CA1085080808

Gene: FLT4

Linked Data

• dbSNP Id: rs1761564985
• gnomAD v3: 5-180602485-T-C
• gnomAD v4: 5-180602485-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602485T>C , CM000667.2:g.180602485T>C	GRCh38
NC_000005.9:g.180029485T>C , CM000667.1:g.180029485T>C	GRCh37
NC_000005.8:g.179962091T>C	NCBI36
NG_011536.1:g.52140A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*707A>G MANE Select	ENSP00000261937.6:n.*707A>G
ENST00000261937.10:c.*707A>G	ENSP00000261937.6:n.*707A>G
NM_182925.4:c.*707A>G	NP_891555.2:n.*707A>G
XM_011534477.1:c.*707A>G	XP_011532779.1:n.*707A>G
XM_011534478.1:c.*707A>G	XP_011532780.1:n.*707A>G
XM_011534482.1:c.*707A>G	XP_011532784.1:n.*707A>G
XM_011534483.1:c.*707A>G	XP_011532785.1:n.*707A>G
XM_011534484.1:c.*707A>G	XP_011532786.1:n.*707A>G
XM_011534478.3:c.*707A>G	XP_011532780.1:n.*707A>G
XM_011534484.2:c.*707A>G	XP_011532786.1:n.*707A>G
XM_017009263.1:c.*945A>G	XP_016864752.1:n.*945A>G
XM_017009268.1:c.*707A>G	XP_016864757.1:n.*707A>G
XR_001742050.2:n.5289A>G
NM_182925.5:c.*707A>G MANE Select	NP_891555.2:n.*707A>G