Canonical Allele Identifier: CA362498058

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036994G>T (hg19) ; chr5:g.180609994G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609994G>T , CM000667.2:g.180609994G>T	GRCh38
NC_000005.9:g.180036994G>T , CM000667.1:g.180036994G>T	GRCh37
NC_000005.8:g.179969600G>T	NCBI36
NG_011536.1:g.44631C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3718C>A MANE Select	ENSP00000261937.6:p.Leu1240Met
ENST00000261937.10:c.3718C>A	ENSP00000261937.6:p.Leu1240Met
ENST00000393347.7:c.3718C>A	ENSP00000377016.3:p.Leu1240Met
ENST00000502603.5:n.418C>A
ENST00000502649.5:c.3718C>A	ENSP00000426057.1:p.Leu1240Met
ENST00000507059.5:n.4068C>A
ENST00000619105.4:c.*2661C>A	ENSP00000481134.1:n.*2661C>A
NM_002020.4:c.3718C>A	NP_002011.2:p.Leu1240Met
NM_182925.4:c.3718C>A	NP_891555.2:p.Leu1240Met
XM_011534477.1:c.3967C>A	XP_011532779.1:p.Leu1323Met
XM_011534478.1:c.3949C>A	XP_011532780.1:p.Leu1317Met
XM_011534479.1:c.3967C>A	XP_011532781.1:p.Leu1323Met
XM_011534480.1:c.3967C>A	XP_011532782.1:p.Leu1323Met
XM_011534481.1:c.3967C>A	XP_011532783.1:p.Leu1323Met
XM_011534482.1:c.3736C>A	XP_011532784.1:p.Leu1246Met
XM_011534483.1:c.3658C>A	XP_011532785.1:p.Leu1220Met
XM_011534484.1:c.3259C>A	XP_011532786.1:p.Leu1087Met
XR_941095.1:n.4004C>A
NM_001354989.1:c.3718C>A	NP_001341918.1:p.Leu1240Met
XM_011534478.3:c.3949C>A	XP_011532780.1:p.Leu1317Met
XM_011534484.2:c.3259C>A	XP_011532786.1:p.Leu1087Met
XM_017009263.1:c.3949C>A	XP_016864752.1:p.Leu1317Met
XM_017009264.2:c.3949C>A	XP_016864753.1:p.Leu1317Met
XM_017009265.1:c.3949C>A	XP_016864754.1:p.Leu1317Met
XM_017009266.1:c.3949C>A	XP_016864755.1:p.Leu1317Met
XM_017009267.2:c.3949C>A	XP_016864756.1:p.Leu1317Met
XM_017009268.1:c.3640C>A	XP_016864757.1:p.Leu1214Met
XR_001742050.2:n.4208C>A
NM_182925.5:c.3718C>A MANE Select	NP_891555.2:p.Leu1240Met
NM_001354989.2:c.3718C>A	NP_001341918.1:p.Leu1240Met
NM_002020.5:c.3718C>A	NP_002011.2:p.Leu1240Met