Canonical Allele Identifier: CA362500286
Gene: FLT4 HGNC NCBI

Linked Data

dbSNP Id: rs2127797426

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.180614145C>A , CM000667.2:g.180614145C>A GRCh38
NC_000005.9:g.180041145C>A , CM000667.1:g.180041145C>A GRCh37
NC_000005.8:g.179973751C>A NCBI36
NG_011536.1:g.40480G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261937.11:c.3254G>T MANE Select ENSP00000261937.6:p.Ser1085Ile
ENST00000261937.10:c.3254G>T ENSP00000261937.6:p.Ser1085Ile
ENST00000393347.7:c.3254G>T ENSP00000377016.3:p.Ser1085Ile
ENST00000502649.5:c.3254G>T ENSP00000426057.1:p.Ser1085Ile
ENST00000507059.5:n.2647G>T
ENST00000512795.1:c.368G>T ENSP00000421535.1:p.Ser123Ile
ENST00000514810.1:n.621G>T
ENST00000619105.4:c.*2197G>T ENSP00000481134.1:n.*2197G>T
NM_002020.4:c.3254G>T NP_002011.2:p.Ser1085Ile
NM_182925.4:c.3254G>T NP_891555.2:p.Ser1085Ile
XM_011534477.1:c.3503G>T XP_011532779.1:p.Ser1168Ile
XM_011534478.1:c.3485G>T XP_011532780.1:p.Ser1162Ile
XM_011534479.1:c.3503G>T XP_011532781.1:p.Ser1168Ile
XM_011534480.1:c.3503G>T XP_011532782.1:p.Ser1168Ile
XM_011534481.1:c.3503G>T XP_011532783.1:p.Ser1168Ile
XM_011534482.1:c.3272G>T XP_011532784.1:p.Ser1091Ile
XM_011534483.1:c.3194G>T XP_011532785.1:p.Ser1065Ile
XM_011534484.1:c.2795G>T XP_011532786.1:p.Ser932Ile
XR_941095.1:n.3515G>T
NM_001354989.1:c.3254G>T NP_001341918.1:p.Ser1085Ile
XM_011534478.3:c.3485G>T XP_011532780.1:p.Ser1162Ile
XM_011534484.2:c.2795G>T XP_011532786.1:p.Ser932Ile
XM_017009263.1:c.3485G>T XP_016864752.1:p.Ser1162Ile
XM_017009264.2:c.3485G>T XP_016864753.1:p.Ser1162Ile
XM_017009265.1:c.3485G>T XP_016864754.1:p.Ser1162Ile
XM_017009266.1:c.3485G>T XP_016864755.1:p.Ser1162Ile
XM_017009267.2:c.3485G>T XP_016864756.1:p.Ser1162Ile
XM_017009268.1:c.3176G>T XP_016864757.1:p.Ser1059Ile
XR_001742050.2:n.3719G>T
NM_182925.5:c.3254G>T MANE Select NP_891555.2:p.Ser1085Ile
NM_001354989.2:c.3254G>T NP_001341918.1:p.Ser1085Ile
NM_002020.5:c.3254G>T NP_002011.2:p.Ser1085Ile