Canonical Allele Identifier: CA362495946
Gene: FLT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603307G>T , CM000667.2:g.180603307G>T GRCh38
NC_000005.9:g.180030307G>T , CM000667.1:g.180030307G>T GRCh37
NC_000005.8:g.179962913G>T NCBI36
NG_011536.1:g.51318C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3977C>A MANE Select ENSP00000261937.6:p.Ala1326Asp
ENST00000261937.10:c.3977C>A ENSP00000261937.6:p.Ala1326Asp
ENST00000502603.5:n.677C>A
NM_182925.4:c.3977C>A NP_891555.2:p.Ala1326Asp
XM_011534477.1:c.4226C>A XP_011532779.1:p.Ala1409Asp
XM_011534478.1:c.4208C>A XP_011532780.1:p.Ala1403Asp
XM_011534479.1:c.*123C>A XP_011532781.1:n.*123C>A
XM_011534482.1:c.3995C>A XP_011532784.1:p.Ala1332Asp
XM_011534483.1:c.3917C>A XP_011532785.1:p.Ala1306Asp
XM_011534484.1:c.3518C>A XP_011532786.1:p.Ala1173Asp
XR_941095.1:n.4263C>A
XM_011534478.3:c.4208C>A XP_011532780.1:p.Ala1403Asp
XM_011534484.2:c.3518C>A XP_011532786.1:p.Ala1173Asp
XM_017009263.1:c.*123C>A XP_016864752.1:n.*123C>A
XM_017009268.1:c.3899C>A XP_016864757.1:p.Ala1300Asp
XR_001742050.2:n.4467C>A
NM_182925.5:c.3977C>A MANE Select NP_891555.2:p.Ala1326Asp