Canonical Allele Identifier: CA1604717392
Gene: FLT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180609796_180609798delinsGAC , CM000667.2:g.180609796_180609798delinsGAC GRCh38
NC_000005.9:g.180036796_180036798delinsGAC , CM000667.1:g.180036796_180036798delinsGAC GRCh37
NC_000005.8:g.179969402_179969404delinsGAC NCBI36
NG_011536.1:g.44827_44829delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3807+107_3807+109delinsGTC MANE Select ENSP00000261937.6:n.3807+107_3807+109delinsGTC
ENST00000261937.10:c.3807+107_3807+109delinsGTC ENSP00000261937.6:n.3807+107_3807+109delinsGTC
ENST00000393347.7:c.3807+107_3807+109delinsGTC ENSP00000377016.3:n.3807+107_3807+109delinsGTC
ENST00000502603.5:n.507+107_507+109delinsGTC
ENST00000502649.5:c.3807+107_3807+109delinsGTC ENSP00000426057.1:n.3807+107_3807+109delinsGTC
ENST00000507059.5:n.4264_4266delinsGTC
ENST00000619105.4:c.*2750+107_*2750+109delinsGTC ENSP00000481134.1:n.*2750+107_*2750+109delinsGTC
NM_002020.4:c.3807+107_3807+109delinsGTC NP_002011.2:n.3807+107_3807+109delinsGTC
NM_182925.4:c.3807+107_3807+109delinsGTC NP_891555.2:n.3807+107_3807+109delinsGTC
XM_011534477.1:c.4056+107_4056+109delinsGTC XP_011532779.1:n.4056+107_4056+109delinsGTC
XM_011534478.1:c.4038+107_4038+109delinsGTC XP_011532780.1:n.4038+107_4038+109delinsGTC
XM_011534479.1:c.4056+107_4056+109delinsGTC XP_011532781.1:n.4056+107_4056+109delinsGTC
XM_011534480.1:c.4056+107_4056+109delinsGTC XP_011532782.1:n.4056+107_4056+109delinsGTC
XM_011534481.1:c.4056+107_4056+109delinsGTC XP_011532783.1:n.4056+107_4056+109delinsGTC
XM_011534482.1:c.3825+107_3825+109delinsGTC XP_011532784.1:n.3825+107_3825+109delinsGTC
XM_011534483.1:c.3747+107_3747+109delinsGTC XP_011532785.1:n.3747+107_3747+109delinsGTC
XM_011534484.1:c.3348+107_3348+109delinsGTC XP_011532786.1:n.3348+107_3348+109delinsGTC
XR_941095.1:n.4093+107_4093+109delinsGTC
NM_001354989.1:c.3807+107_3807+109delinsGTC NP_001341918.1:n.3807+107_3807+109delinsGTC
XM_011534478.3:c.4038+107_4038+109delinsGTC XP_011532780.1:n.4038+107_4038+109delinsGTC
XM_011534484.2:c.3348+107_3348+109delinsGTC XP_011532786.1:n.3348+107_3348+109delinsGTC
XM_017009263.1:c.4038+107_4038+109delinsGTC XP_016864752.1:n.4038+107_4038+109delinsGTC
XM_017009264.2:c.4038+107_4038+109delinsGTC XP_016864753.1:n.4038+107_4038+109delinsGTC
XM_017009265.1:c.4038+107_4038+109delinsGTC XP_016864754.1:n.4038+107_4038+109delinsGTC
XM_017009266.1:c.4038+107_4038+109delinsGTC XP_016864755.1:n.4038+107_4038+109delinsGTC
XM_017009267.2:c.4038+107_4038+109delinsGTC XP_016864756.1:n.4038+107_4038+109delinsGTC
XM_017009268.1:c.3729+107_3729+109delinsGTC XP_016864757.1:n.3729+107_3729+109delinsGTC
XR_001742050.2:n.4297+107_4297+109delinsGTC
NM_182925.5:c.3807+107_3807+109delinsGTC MANE Select NP_891555.2:n.3807+107_3807+109delinsGTC
NM_001354989.2:c.3807+107_3807+109delinsGTC NP_001341918.1:n.3807+107_3807+109delinsGTC
NM_002020.5:c.3807+107_3807+109delinsGTC NP_002011.2:n.3807+107_3807+109delinsGTC