Canonical Allele Identifier: CA645544773
Gene: FLT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603295_180603296insCCTG , CM000667.2:g.180603295_180603296insCCTG GRCh38
NC_000005.9:g.180030295_180030296insCCTG , CM000667.1:g.180030295_180030296insCCTG GRCh37
NC_000005.8:g.179962901_179962902insCCTG NCBI36
NG_011536.1:g.51329_51330insCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3988_3989insCAGG MANE Select ENSP00000261937.6:p.Gln1330ProfsTer?
ENST00000261937.10:c.3988_3989insCAGG ENSP00000261937.6:p.Gln1330ProfsTer?
ENST00000502603.5:n.688_689insCAGG
NM_182925.4:c.3988_3989insCAGG NP_891555.2:p.Gln1330ProfsTer?
XM_011534477.1:c.4237_4238insCAGG XP_011532779.1:p.Gln1413ProfsTer?
XM_011534478.1:c.4219_4220insCAGG XP_011532780.1:p.Gln1407ProfsTer?
XM_011534482.1:c.4006_4007insCAGG XP_011532784.1:p.Gln1336ProfsTer?
XM_011534483.1:c.3928_3929insCAGG XP_011532785.1:p.Gln1310ProfsTer?
XM_011534484.1:c.3529_3530insCAGG XP_011532786.1:p.Gln1177ProfsTer?
XR_941095.1:n.4274_4275insCAGG
XM_011534478.3:c.4219_4220insCAGG XP_011532780.1:p.Gln1407ProfsTer?
XM_011534484.2:c.3529_3530insCAGG XP_011532786.1:p.Gln1177ProfsTer?
XM_017009263.1:c.*134_*135insCAGG XP_016864752.1:n.*134_*135insCAGG
XM_017009268.1:c.3910_3911insCAGG XP_016864757.1:p.Gln1304ProfsTer?
XR_001742050.2:n.4478_4479insCAGG
NM_182925.5:c.3988_3989insCAGG MANE Select NP_891555.2:p.Gln1330ProfsTer?