Canonical Allele Identifier: CA448099112

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030366C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603366C>A , CM000667.2:g.180603366C>A	GRCh38
NC_000005.9:g.180030366C>A , CM000667.1:g.180030366C>A	GRCh37
NC_000005.8:g.179962972C>A	NCBI36
NG_011536.1:g.51259G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3918G>T MANE Select	ENSP00000261937.6:p.Val1306=
ENST00000261937.10:c.3918G>T	ENSP00000261937.6:p.Val1306=
ENST00000502603.5:n.618G>T
NM_182925.4:c.3918G>T	NP_891555.2:p.Val1306=
XM_011534477.1:c.4167G>T	XP_011532779.1:p.Val1389=
XM_011534478.1:c.4149G>T	XP_011532780.1:p.Val1383=
XM_011534479.1:c.*64G>T	XP_011532781.1:n.*64G>T
XM_011534482.1:c.3936G>T	XP_011532784.1:p.Val1312=
XM_011534483.1:c.3858G>T	XP_011532785.1:p.Val1286=
XM_011534484.1:c.3459G>T	XP_011532786.1:p.Val1153=
XR_941095.1:n.4204G>T
XM_011534478.3:c.4149G>T	XP_011532780.1:p.Val1383=
XM_011534484.2:c.3459G>T	XP_011532786.1:p.Val1153=
XM_017009263.1:c.*64G>T	XP_016864752.1:n.*64G>T
XM_017009268.1:c.3840G>T	XP_016864757.1:p.Val1280=
XR_001742050.2:n.4408G>T
NM_182925.5:c.3918G>T MANE Select	NP_891555.2:p.Val1306=