Canonical Allele Identifier: CA2532437979
Gene: FLT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603193del , CM000667.2:g.180603193del GRCh38
NC_000005.9:g.180030193del , CM000667.1:g.180030193del GRCh37
NC_000005.8:g.179962799del NCBI36
NG_011536.1:g.51433del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.4092del MANE Select ENSP00000261937.6:p.Ter1364=
ENST00000261937.10:c.4092del ENSP00000261937.6:p.Ter1364=
ENST00000502603.5:n.792del
NM_182925.4:c.4092del NP_891555.2:p.Ter1364=
XM_011534477.1:c.4341del XP_011532779.1:p.Ter1447=
XM_011534478.1:c.4323del XP_011532780.1:p.Ter1441=
XM_011534482.1:c.4110del XP_011532784.1:p.Ter1370=
XM_011534483.1:c.4032del XP_011532785.1:p.Ter1344=
XM_011534484.1:c.3633del XP_011532786.1:p.Ter1211=
XR_941095.1:n.4378del
XM_011534478.3:c.4323del XP_011532780.1:p.Ter1441=
XM_011534484.2:c.3633del XP_011532786.1:p.Ter1211=
XM_017009263.1:c.*238del XP_016864752.1:n.*238del
XM_017009268.1:c.4014del XP_016864757.1:p.Ter1338=
XR_001742050.2:n.4582del
NM_182925.5:c.4092del MANE Select NP_891555.2:p.Ter1364=