Canonical Allele Identifier: CA448099004

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030234G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603234G>T , CM000667.2:g.180603234G>T	GRCh38
NC_000005.9:g.180030234G>T , CM000667.1:g.180030234G>T	GRCh37
NC_000005.8:g.179962840G>T	NCBI36
NG_011536.1:g.51391C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4050C>A MANE Select	ENSP00000261937.6:p.Ser1350=
ENST00000261937.10:c.4050C>A	ENSP00000261937.6:p.Ser1350=
ENST00000502603.5:n.750C>A
NM_182925.4:c.4050C>A	NP_891555.2:p.Ser1350=
XM_011534477.1:c.4299C>A	XP_011532779.1:p.Ser1433=
XM_011534478.1:c.4281C>A	XP_011532780.1:p.Ser1427=
XM_011534482.1:c.4068C>A	XP_011532784.1:p.Ser1356=
XM_011534483.1:c.3990C>A	XP_011532785.1:p.Ser1330=
XM_011534484.1:c.3591C>A	XP_011532786.1:p.Ser1197=
XR_941095.1:n.4336C>A
XM_011534478.3:c.4281C>A	XP_011532780.1:p.Ser1427=
XM_011534484.2:c.3591C>A	XP_011532786.1:p.Ser1197=
XM_017009263.1:c.*196C>A	XP_016864752.1:n.*196C>A
XM_017009268.1:c.3972C>A	XP_016864757.1:p.Ser1324=
XR_001742050.2:n.4540C>A
NM_182925.5:c.4050C>A MANE Select	NP_891555.2:p.Ser1350=