Canonical Allele Identifier: CA448099054

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030300T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603300T>A , CM000667.2:g.180603300T>A	GRCh38
NC_000005.9:g.180030300T>A , CM000667.1:g.180030300T>A	GRCh37
NC_000005.8:g.179962906T>A	NCBI36
NG_011536.1:g.51325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3984A>T MANE Select	ENSP00000261937.6:p.Gly1328=
ENST00000261937.10:c.3984A>T	ENSP00000261937.6:p.Gly1328=
ENST00000502603.5:n.684A>T
NM_182925.4:c.3984A>T	NP_891555.2:p.Gly1328=
XM_011534477.1:c.4233A>T	XP_011532779.1:p.Gly1411=
XM_011534478.1:c.4215A>T	XP_011532780.1:p.Gly1405=
XM_011534482.1:c.4002A>T	XP_011532784.1:p.Gly1334=
XM_011534483.1:c.3924A>T	XP_011532785.1:p.Gly1308=
XM_011534484.1:c.3525A>T	XP_011532786.1:p.Gly1175=
XR_941095.1:n.4270A>T
XM_011534478.3:c.4215A>T	XP_011532780.1:p.Gly1405=
XM_011534484.2:c.3525A>T	XP_011532786.1:p.Gly1175=
XM_017009263.1:c.*130A>T	XP_016864752.1:n.*130A>T
XM_017009268.1:c.3906A>T	XP_016864757.1:p.Gly1302=
XR_001742050.2:n.4474A>T
NM_182925.5:c.3984A>T MANE Select	NP_891555.2:p.Gly1328=