Canonical Allele Identifier: CA3605708
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs762732020

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609973G>A , CM000667.2:g.180609973G>A GRCh38
NC_000005.9:g.180036973G>A , CM000667.1:g.180036973G>A GRCh37
NC_000005.8:g.179969579G>A NCBI36
NG_011536.1:g.44652C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3739C>T MANE Select ENSP00000261937.6:p.Arg1247Cys
ENST00000261937.10:c.3739C>T ENSP00000261937.6:p.Arg1247Cys
ENST00000393347.7:c.3739C>T ENSP00000377016.3:p.Arg1247Cys
ENST00000502603.5:n.439C>T
ENST00000502649.5:c.3739C>T ENSP00000426057.1:p.Arg1247Cys
ENST00000507059.5:n.4089C>T
ENST00000619105.4:c.*2682C>T ENSP00000481134.1:n.*2682C>T
NM_002020.4:c.3739C>T NP_002011.2:p.Arg1247Cys
NM_182925.4:c.3739C>T NP_891555.2:p.Arg1247Cys
XM_011534477.1:c.3988C>T XP_011532779.1:p.Arg1330Cys
XM_011534478.1:c.3970C>T XP_011532780.1:p.Arg1324Cys
XM_011534479.1:c.3988C>T XP_011532781.1:p.Arg1330Cys
XM_011534480.1:c.3988C>T XP_011532782.1:p.Arg1330Cys
XM_011534481.1:c.3988C>T XP_011532783.1:p.Arg1330Cys
XM_011534482.1:c.3757C>T XP_011532784.1:p.Arg1253Cys
XM_011534483.1:c.3679C>T XP_011532785.1:p.Arg1227Cys
XM_011534484.1:c.3280C>T XP_011532786.1:p.Arg1094Cys
XR_941095.1:n.4025C>T
NM_001354989.1:c.3739C>T NP_001341918.1:p.Arg1247Cys
XM_011534478.3:c.3970C>T XP_011532780.1:p.Arg1324Cys
XM_011534484.2:c.3280C>T XP_011532786.1:p.Arg1094Cys
XM_017009263.1:c.3970C>T XP_016864752.1:p.Arg1324Cys
XM_017009264.2:c.3970C>T XP_016864753.1:p.Arg1324Cys
XM_017009265.1:c.3970C>T XP_016864754.1:p.Arg1324Cys
XM_017009266.1:c.3970C>T XP_016864755.1:p.Arg1324Cys
XM_017009267.2:c.3970C>T XP_016864756.1:p.Arg1324Cys
XM_017009268.1:c.3661C>T XP_016864757.1:p.Arg1221Cys
XR_001742050.2:n.4229C>T
NM_182925.5:c.3739C>T MANE Select NP_891555.2:p.Arg1247Cys
NM_001354989.2:c.3739C>T NP_001341918.1:p.Arg1247Cys
NM_002020.5:c.3739C>T NP_002011.2:p.Arg1247Cys