Canonical Allele Identifier: CA362495609

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030259T>A (hg19) ; chr5:g.180603259T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603259T>A , CM000667.2:g.180603259T>A	GRCh38
NC_000005.9:g.180030259T>A , CM000667.1:g.180030259T>A	GRCh37
NC_000005.8:g.179962865T>A	NCBI36
NG_011536.1:g.51366A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4025A>T MANE Select	ENSP00000261937.6:p.Glu1342Val
ENST00000261937.10:c.4025A>T	ENSP00000261937.6:p.Glu1342Val
ENST00000502603.5:n.725A>T
NM_182925.4:c.4025A>T	NP_891555.2:p.Glu1342Val
XM_011534477.1:c.4274A>T	XP_011532779.1:p.Glu1425Val
XM_011534478.1:c.4256A>T	XP_011532780.1:p.Glu1419Val
XM_011534482.1:c.4043A>T	XP_011532784.1:p.Glu1348Val
XM_011534483.1:c.3965A>T	XP_011532785.1:p.Glu1322Val
XM_011534484.1:c.3566A>T	XP_011532786.1:p.Glu1189Val
XR_941095.1:n.4311A>T
XM_011534478.3:c.4256A>T	XP_011532780.1:p.Glu1419Val
XM_011534484.2:c.3566A>T	XP_011532786.1:p.Glu1189Val
XM_017009263.1:c.*171A>T	XP_016864752.1:n.*171A>T
XM_017009268.1:c.3947A>T	XP_016864757.1:p.Glu1316Val
XR_001742050.2:n.4515A>T
NM_182925.5:c.4025A>T MANE Select	NP_891555.2:p.Glu1342Val