Canonical Allele Identifier: CA3605707
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs773030985

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609970C>T , CM000667.2:g.180609970C>T GRCh38
NC_000005.9:g.180036970C>T , CM000667.1:g.180036970C>T GRCh37
NC_000005.8:g.179969576C>T NCBI36
NG_011536.1:g.44655G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3742G>A MANE Select ENSP00000261937.6:p.Gly1248Ser
ENST00000261937.10:c.3742G>A ENSP00000261937.6:p.Gly1248Ser
ENST00000393347.7:c.3742G>A ENSP00000377016.3:p.Gly1248Ser
ENST00000502603.5:n.442G>A
ENST00000502649.5:c.3742G>A ENSP00000426057.1:p.Gly1248Ser
ENST00000507059.5:n.4092G>A
ENST00000619105.4:c.*2685G>A ENSP00000481134.1:n.*2685G>A
NM_002020.4:c.3742G>A NP_002011.2:p.Gly1248Ser
NM_182925.4:c.3742G>A NP_891555.2:p.Gly1248Ser
XM_011534477.1:c.3991G>A XP_011532779.1:p.Gly1331Ser
XM_011534478.1:c.3973G>A XP_011532780.1:p.Gly1325Ser
XM_011534479.1:c.3991G>A XP_011532781.1:p.Gly1331Ser
XM_011534480.1:c.3991G>A XP_011532782.1:p.Gly1331Ser
XM_011534481.1:c.3991G>A XP_011532783.1:p.Gly1331Ser
XM_011534482.1:c.3760G>A XP_011532784.1:p.Gly1254Ser
XM_011534483.1:c.3682G>A XP_011532785.1:p.Gly1228Ser
XM_011534484.1:c.3283G>A XP_011532786.1:p.Gly1095Ser
XR_941095.1:n.4028G>A
NM_001354989.1:c.3742G>A NP_001341918.1:p.Gly1248Ser
XM_011534478.3:c.3973G>A XP_011532780.1:p.Gly1325Ser
XM_011534484.2:c.3283G>A XP_011532786.1:p.Gly1095Ser
XM_017009263.1:c.3973G>A XP_016864752.1:p.Gly1325Ser
XM_017009264.2:c.3973G>A XP_016864753.1:p.Gly1325Ser
XM_017009265.1:c.3973G>A XP_016864754.1:p.Gly1325Ser
XM_017009266.1:c.3973G>A XP_016864755.1:p.Gly1325Ser
XM_017009267.2:c.3973G>A XP_016864756.1:p.Gly1325Ser
XM_017009268.1:c.3664G>A XP_016864757.1:p.Gly1222Ser
XR_001742050.2:n.4232G>A
NM_182925.5:c.3742G>A MANE Select NP_891555.2:p.Gly1248Ser
NM_001354989.2:c.3742G>A NP_001341918.1:p.Gly1248Ser
NM_002020.5:c.3742G>A NP_002011.2:p.Gly1248Ser