Canonical Allele Identifier: CA448099031

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030258C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603258C>T , CM000667.2:g.180603258C>T	GRCh38
NC_000005.9:g.180030258C>T , CM000667.1:g.180030258C>T	GRCh37
NC_000005.8:g.179962864C>T	NCBI36
NG_011536.1:g.51367G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4026G>A MANE Select	ENSP00000261937.6:p.Glu1342=
ENST00000261937.10:c.4026G>A	ENSP00000261937.6:p.Glu1342=
ENST00000502603.5:n.726G>A
NM_182925.4:c.4026G>A	NP_891555.2:p.Glu1342=
XM_011534477.1:c.4275G>A	XP_011532779.1:p.Glu1425=
XM_011534478.1:c.4257G>A	XP_011532780.1:p.Glu1419=
XM_011534482.1:c.4044G>A	XP_011532784.1:p.Glu1348=
XM_011534483.1:c.3966G>A	XP_011532785.1:p.Glu1322=
XM_011534484.1:c.3567G>A	XP_011532786.1:p.Glu1189=
XR_941095.1:n.4312G>A
XM_011534478.3:c.4257G>A	XP_011532780.1:p.Glu1419=
XM_011534484.2:c.3567G>A	XP_011532786.1:p.Glu1189=
XM_017009263.1:c.*172G>A	XP_016864752.1:n.*172G>A
XM_017009268.1:c.3948G>A	XP_016864757.1:p.Glu1316=
XR_001742050.2:n.4516G>A
NM_182925.5:c.4026G>A MANE Select	NP_891555.2:p.Glu1342=