Canonical Allele Identifier: CA362497826

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609040T>G , CM000667.2:g.180609040T>G	GRCh38
NC_000005.9:g.180036040T>G , CM000667.1:g.180036040T>G	GRCh37
NC_000005.8:g.179968646T>G	NCBI36
NG_011536.1:g.45585A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_182925.5:c.3821A>C MANE Select	NP_891555.2:p.Asp1274Ala
ENST00000261937.11:c.3821A>C MANE Select	ENSP00000261937.6:p.Asp1274Ala
NM_001354989.1:c.3821A>C	NP_001341918.1:p.Asp1274Ala
NM_001354989.2:c.3821A>C	NP_001341918.1:p.Asp1274Ala
NM_002020.4:c.3821A>C	NP_002011.2:p.Asp1274Ala
NM_002020.5:c.3821A>C	NP_002011.2:p.Asp1274Ala
NM_182925.4:c.3821A>C	NP_891555.2:p.Asp1274Ala
ENST00000261937.10:c.3821A>C	ENSP00000261937.6:p.Asp1274Ala
ENST00000393347.7:c.3821A>C	ENSP00000377016.3:p.Asp1274Ala
ENST00000502603.5:n.521A>C
ENST00000502649.5:c.3821A>C	ENSP00000426057.1:p.Asp1274Ala
ENST00000507059.5:n.5022A>C
ENST00000619105.4:c.*2764A>C	ENSP00000481134.1:n.*2764A>C
XM_011534477.1:c.4070A>C	XP_011532779.1:p.Asp1357Ala
XM_011534478.1:c.4052A>C	XP_011532780.1:p.Asp1351Ala
XM_011534478.3:c.4052A>C	XP_011532780.1:p.Asp1351Ala
XM_011534479.1:c.4143A>C	XP_011532781.1:p.Arg1381Ser
XM_011534480.1:c.4143A>C	XP_011532782.1:p.Arg1381Ser
XM_011534481.1:c.4070A>C	XP_011532783.1:p.Asp1357Ala
XM_011534482.1:c.3839A>C	XP_011532784.1:p.Asp1280Ala
XM_011534483.1:c.3761A>C	XP_011532785.1:p.Asp1254Ala
XM_011534484.1:c.3362A>C	XP_011532786.1:p.Asp1121Ala
XM_011534484.2:c.3362A>C	XP_011532786.1:p.Asp1121Ala
XM_017009263.1:c.4125A>C	XP_016864752.1:p.Arg1375Ser
XM_017009264.2:c.4125A>C	XP_016864753.1:p.Arg1375Ser
XM_017009265.1:c.4125A>C	XP_016864754.1:p.Arg1375Ser
XM_017009266.1:c.4052A>C	XP_016864755.1:p.Asp1351Ala
XM_017009267.2:c.4052A>C	XP_016864756.1:p.Asp1351Ala
XM_017009268.1:c.3743A>C	XP_016864757.1:p.Asp1248Ala
XR_001742050.2:n.4311A>C
XR_941095.1:n.4107A>C