Canonical Allele Identifier: CA362498054
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs1270698155

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609993A>C , CM000667.2:g.180609993A>C GRCh38
NC_000005.9:g.180036993A>C , CM000667.1:g.180036993A>C GRCh37
NC_000005.8:g.179969599A>C NCBI36
NG_011536.1:g.44632T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3719T>G MANE Select ENSP00000261937.6:p.Leu1240Arg
ENST00000261937.10:c.3719T>G ENSP00000261937.6:p.Leu1240Arg
ENST00000393347.7:c.3719T>G ENSP00000377016.3:p.Leu1240Arg
ENST00000502603.5:n.419T>G
ENST00000502649.5:c.3719T>G ENSP00000426057.1:p.Leu1240Arg
ENST00000507059.5:n.4069T>G
ENST00000619105.4:c.*2662T>G ENSP00000481134.1:n.*2662T>G
NM_002020.4:c.3719T>G NP_002011.2:p.Leu1240Arg
NM_182925.4:c.3719T>G NP_891555.2:p.Leu1240Arg
XM_011534477.1:c.3968T>G XP_011532779.1:p.Leu1323Arg
XM_011534478.1:c.3950T>G XP_011532780.1:p.Leu1317Arg
XM_011534479.1:c.3968T>G XP_011532781.1:p.Leu1323Arg
XM_011534480.1:c.3968T>G XP_011532782.1:p.Leu1323Arg
XM_011534481.1:c.3968T>G XP_011532783.1:p.Leu1323Arg
XM_011534482.1:c.3737T>G XP_011532784.1:p.Leu1246Arg
XM_011534483.1:c.3659T>G XP_011532785.1:p.Leu1220Arg
XM_011534484.1:c.3260T>G XP_011532786.1:p.Leu1087Arg
XR_941095.1:n.4005T>G
NM_001354989.1:c.3719T>G NP_001341918.1:p.Leu1240Arg
XM_011534478.3:c.3950T>G XP_011532780.1:p.Leu1317Arg
XM_011534484.2:c.3260T>G XP_011532786.1:p.Leu1087Arg
XM_017009263.1:c.3950T>G XP_016864752.1:p.Leu1317Arg
XM_017009264.2:c.3950T>G XP_016864753.1:p.Leu1317Arg
XM_017009265.1:c.3950T>G XP_016864754.1:p.Leu1317Arg
XM_017009266.1:c.3950T>G XP_016864755.1:p.Leu1317Arg
XM_017009267.2:c.3950T>G XP_016864756.1:p.Leu1317Arg
XM_017009268.1:c.3641T>G XP_016864757.1:p.Leu1214Arg
XR_001742050.2:n.4209T>G
NM_182925.5:c.3719T>G MANE Select NP_891555.2:p.Leu1240Arg
NM_001354989.2:c.3719T>G NP_001341918.1:p.Leu1240Arg
NM_002020.5:c.3719T>G NP_002011.2:p.Leu1240Arg