Canonical Allele Identifier: CA448099044

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030276C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603276C>T , CM000667.2:g.180603276C>T	GRCh38
NC_000005.9:g.180030276C>T , CM000667.1:g.180030276C>T	GRCh37
NC_000005.8:g.179962882C>T	NCBI36
NG_011536.1:g.51349G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4008G>A MANE Select	ENSP00000261937.6:p.Glu1336=
ENST00000261937.10:c.4008G>A	ENSP00000261937.6:p.Glu1336=
ENST00000502603.5:n.708G>A
NM_182925.4:c.4008G>A	NP_891555.2:p.Glu1336=
XM_011534477.1:c.4257G>A	XP_011532779.1:p.Glu1419=
XM_011534478.1:c.4239G>A	XP_011532780.1:p.Glu1413=
XM_011534482.1:c.4026G>A	XP_011532784.1:p.Glu1342=
XM_011534483.1:c.3948G>A	XP_011532785.1:p.Glu1316=
XM_011534484.1:c.3549G>A	XP_011532786.1:p.Glu1183=
XR_941095.1:n.4294G>A
XM_011534478.3:c.4239G>A	XP_011532780.1:p.Glu1413=
XM_011534484.2:c.3549G>A	XP_011532786.1:p.Glu1183=
XM_017009263.1:c.*154G>A	XP_016864752.1:n.*154G>A
XM_017009268.1:c.3930G>A	XP_016864757.1:p.Glu1310=
XR_001742050.2:n.4498G>A
NM_182925.5:c.4008G>A MANE Select	NP_891555.2:p.Glu1336=