Canonical Allele Identifier: CA645544776
Gene: FLT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609999_180610000delinsAA , CM000667.2:g.180609999_180610000delinsAA GRCh38
NC_000005.9:g.180036999_180037000delinsAA , CM000667.1:g.180036999_180037000delinsAA GRCh37
NC_000005.8:g.179969605_179969606delinsAA NCBI36
NG_011536.1:g.44625_44626delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3712_3713delinsTT MANE Select ENSP00000261937.6:p.Gly1238Leu
ENST00000261937.10:c.3712_3713delinsTT ENSP00000261937.6:p.Gly1238Leu
ENST00000393347.7:c.3712_3713delinsTT ENSP00000377016.3:p.Gly1238Leu
ENST00000502603.5:n.412_413delinsTT
ENST00000502649.5:c.3712_3713delinsTT ENSP00000426057.1:p.Gly1238Leu
ENST00000507059.5:n.4062_4063delinsTT
ENST00000619105.4:c.*2655_*2656delinsTT ENSP00000481134.1:n.*2655_*2656delinsTT
NM_002020.4:c.3712_3713delinsTT NP_002011.2:p.Gly1238Leu
NM_182925.4:c.3712_3713delinsTT NP_891555.2:p.Gly1238Leu
XM_011534477.1:c.3961_3962delinsTT XP_011532779.1:p.Gly1321Leu
XM_011534478.1:c.3943_3944delinsTT XP_011532780.1:p.Gly1315Leu
XM_011534479.1:c.3961_3962delinsTT XP_011532781.1:p.Gly1321Leu
XM_011534480.1:c.3961_3962delinsTT XP_011532782.1:p.Gly1321Leu
XM_011534481.1:c.3961_3962delinsTT XP_011532783.1:p.Gly1321Leu
XM_011534482.1:c.3730_3731delinsTT XP_011532784.1:p.Gly1244Leu
XM_011534483.1:c.3652_3653delinsTT XP_011532785.1:p.Gly1218Leu
XM_011534484.1:c.3253_3254delinsTT XP_011532786.1:p.Gly1085Leu
XR_941095.1:n.3998_3999delinsTT
NM_001354989.1:c.3712_3713delinsTT NP_001341918.1:p.Gly1238Leu
XM_011534478.3:c.3943_3944delinsTT XP_011532780.1:p.Gly1315Leu
XM_011534484.2:c.3253_3254delinsTT XP_011532786.1:p.Gly1085Leu
XM_017009263.1:c.3943_3944delinsTT XP_016864752.1:p.Gly1315Leu
XM_017009264.2:c.3943_3944delinsTT XP_016864753.1:p.Gly1315Leu
XM_017009265.1:c.3943_3944delinsTT XP_016864754.1:p.Gly1315Leu
XM_017009266.1:c.3943_3944delinsTT XP_016864755.1:p.Gly1315Leu
XM_017009267.2:c.3943_3944delinsTT XP_016864756.1:p.Gly1315Leu
XM_017009268.1:c.3634_3635delinsTT XP_016864757.1:p.Gly1212Leu
XR_001742050.2:n.4202_4203delinsTT
NM_182925.5:c.3712_3713delinsTT MANE Select NP_891555.2:p.Gly1238Leu
NM_001354989.2:c.3712_3713delinsTT NP_001341918.1:p.Gly1238Leu
NM_002020.5:c.3712_3713delinsTT NP_002011.2:p.Gly1238Leu