Canonical Allele Identifier: CA362496324
Gene: FLT4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180603377C>T , CM000667.2:g.180603377C>T GRCh38
NC_000005.9:g.180030377C>T , CM000667.1:g.180030377C>T GRCh37
NC_000005.8:g.179962983C>T NCBI36
NG_011536.1:g.51248G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261937.11:c.3907G>A MANE Select ENSP00000261937.6:p.Gly1303Ser
ENST00000261937.10:c.3907G>A ENSP00000261937.6:p.Gly1303Ser
ENST00000502603.5:n.607G>A
NM_182925.4:c.3907G>A NP_891555.2:p.Gly1303Ser
XM_011534477.1:c.4156G>A XP_011532779.1:p.Gly1386Ser
XM_011534478.1:c.4138G>A XP_011532780.1:p.Gly1380Ser
XM_011534479.1:c.*53G>A XP_011532781.1:n.*53G>A
XM_011534482.1:c.3925G>A XP_011532784.1:p.Gly1309Ser
XM_011534483.1:c.3847G>A XP_011532785.1:p.Gly1283Ser
XM_011534484.1:c.3448G>A XP_011532786.1:p.Gly1150Ser
XR_941095.1:n.4193G>A
XM_011534478.3:c.4138G>A XP_011532780.1:p.Gly1380Ser
XM_011534484.2:c.3448G>A XP_011532786.1:p.Gly1150Ser
XM_017009263.1:c.*53G>A XP_016864752.1:n.*53G>A
XM_017009268.1:c.3829G>A XP_016864757.1:p.Gly1277Ser
XR_001742050.2:n.4397G>A
NM_182925.5:c.3907G>A MANE Select NP_891555.2:p.Gly1303Ser