Canonical Allele Identifier: CA1604713505
Gene: FLT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180602474C= , CM000667.2:g.180602474C= GRCh38
NC_000005.9:g.180029474C= , CM000667.1:g.180029474C= GRCh37
NC_000005.8:g.179962080C= NCBI36
NG_011536.1:g.52151G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.*718G= MANE Select ENSP00000261937.6:n.*718G=
ENST00000261937.10:c.*718G= ENSP00000261937.6:n.*718G=
NM_182925.4:c.*718G= NP_891555.2:n.*718G=
XM_011534477.1:c.*718G= XP_011532779.1:n.*718G=
XM_011534478.1:c.*718G= XP_011532780.1:n.*718G=
XM_011534482.1:c.*718G= XP_011532784.1:n.*718G=
XM_011534483.1:c.*718G= XP_011532785.1:n.*718G=
XM_011534484.1:c.*718G= XP_011532786.1:n.*718G=
XM_011534478.3:c.*718G= XP_011532780.1:n.*718G=
XM_011534484.2:c.*718G= XP_011532786.1:n.*718G=
XM_017009263.1:c.*956G= XP_016864752.1:n.*956G=
XM_017009268.1:c.*718G= XP_016864757.1:n.*718G=
XR_001742050.2:n.5300G=
NM_182925.5:c.*718G= MANE Select NP_891555.2:n.*718G=