Canonical Allele Identifier: CA362495925

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030301C>T (hg19) ; chr5:g.180603301C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603301C>T , CM000667.2:g.180603301C>T	GRCh38
NC_000005.9:g.180030301C>T , CM000667.1:g.180030301C>T	GRCh37
NC_000005.8:g.179962907C>T	NCBI36
NG_011536.1:g.51324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3983G>A MANE Select	ENSP00000261937.6:p.Gly1328Glu
ENST00000261937.10:c.3983G>A	ENSP00000261937.6:p.Gly1328Glu
ENST00000502603.5:n.683G>A
NM_182925.4:c.3983G>A	NP_891555.2:p.Gly1328Glu
XM_011534477.1:c.4232G>A	XP_011532779.1:p.Gly1411Glu
XM_011534478.1:c.4214G>A	XP_011532780.1:p.Gly1405Glu
XM_011534482.1:c.4001G>A	XP_011532784.1:p.Gly1334Glu
XM_011534483.1:c.3923G>A	XP_011532785.1:p.Gly1308Glu
XM_011534484.1:c.3524G>A	XP_011532786.1:p.Gly1175Glu
XR_941095.1:n.4269G>A
XM_011534478.3:c.4214G>A	XP_011532780.1:p.Gly1405Glu
XM_011534484.2:c.3524G>A	XP_011532786.1:p.Gly1175Glu
XM_017009263.1:c.*129G>A	XP_016864752.1:n.*129G>A
XM_017009268.1:c.3905G>A	XP_016864757.1:p.Gly1302Glu
XR_001742050.2:n.4473G>A
NM_182925.5:c.3983G>A MANE Select	NP_891555.2:p.Gly1328Glu