Canonical Allele Identifier: CA448101393

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036988T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609988T>G , CM000667.2:g.180609988T>G	GRCh38
NC_000005.9:g.180036988T>G , CM000667.1:g.180036988T>G	GRCh37
NC_000005.8:g.179969594T>G	NCBI36
NG_011536.1:g.44637A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3724A>C MANE Select	ENSP00000261937.6:p.Arg1242=
ENST00000261937.10:c.3724A>C	ENSP00000261937.6:p.Arg1242=
ENST00000393347.7:c.3724A>C	ENSP00000377016.3:p.Arg1242=
ENST00000502603.5:n.424A>C
ENST00000502649.5:c.3724A>C	ENSP00000426057.1:p.Arg1242=
ENST00000507059.5:n.4074A>C
ENST00000619105.4:c.*2667A>C	ENSP00000481134.1:n.*2667A>C
NM_002020.4:c.3724A>C	NP_002011.2:p.Arg1242=
NM_182925.4:c.3724A>C	NP_891555.2:p.Arg1242=
XM_011534477.1:c.3973A>C	XP_011532779.1:p.Arg1325=
XM_011534478.1:c.3955A>C	XP_011532780.1:p.Arg1319=
XM_011534479.1:c.3973A>C	XP_011532781.1:p.Arg1325=
XM_011534480.1:c.3973A>C	XP_011532782.1:p.Arg1325=
XM_011534481.1:c.3973A>C	XP_011532783.1:p.Arg1325=
XM_011534482.1:c.3742A>C	XP_011532784.1:p.Arg1248=
XM_011534483.1:c.3664A>C	XP_011532785.1:p.Arg1222=
XM_011534484.1:c.3265A>C	XP_011532786.1:p.Arg1089=
XR_941095.1:n.4010A>C
NM_001354989.1:c.3724A>C	NP_001341918.1:p.Arg1242=
XM_011534478.3:c.3955A>C	XP_011532780.1:p.Arg1319=
XM_011534484.2:c.3265A>C	XP_011532786.1:p.Arg1089=
XM_017009263.1:c.3955A>C	XP_016864752.1:p.Arg1319=
XM_017009264.2:c.3955A>C	XP_016864753.1:p.Arg1319=
XM_017009265.1:c.3955A>C	XP_016864754.1:p.Arg1319=
XM_017009266.1:c.3955A>C	XP_016864755.1:p.Arg1319=
XM_017009267.2:c.3955A>C	XP_016864756.1:p.Arg1319=
XM_017009268.1:c.3646A>C	XP_016864757.1:p.Arg1216=
XR_001742050.2:n.4214A>C
NM_182925.5:c.3724A>C MANE Select	NP_891555.2:p.Arg1242=
NM_001354989.2:c.3724A>C	NP_001341918.1:p.Arg1242=
NM_002020.5:c.3724A>C	NP_002011.2:p.Arg1242=