Canonical Allele Identifier: CA362495357

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030204G>T (hg19) ; chr5:g.180603204G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603204G>T , CM000667.2:g.180603204G>T	GRCh38
NC_000005.9:g.180030204G>T , CM000667.1:g.180030204G>T	GRCh37
NC_000005.8:g.179962810G>T	NCBI36
NG_011536.1:g.51421C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4080C>A MANE Select	ENSP00000261937.6:p.Asp1360Glu
ENST00000261937.10:c.4080C>A	ENSP00000261937.6:p.Asp1360Glu
ENST00000502603.5:n.780C>A
NM_182925.4:c.4080C>A	NP_891555.2:p.Asp1360Glu
XM_011534477.1:c.4329C>A	XP_011532779.1:p.Asp1443Glu
XM_011534478.1:c.4311C>A	XP_011532780.1:p.Asp1437Glu
XM_011534482.1:c.4098C>A	XP_011532784.1:p.Asp1366Glu
XM_011534483.1:c.4020C>A	XP_011532785.1:p.Asp1340Glu
XM_011534484.1:c.3621C>A	XP_011532786.1:p.Asp1207Glu
XR_941095.1:n.4366C>A
XM_011534478.3:c.4311C>A	XP_011532780.1:p.Asp1437Glu
XM_011534484.2:c.3621C>A	XP_011532786.1:p.Asp1207Glu
XM_017009263.1:c.*226C>A	XP_016864752.1:n.*226C>A
XM_017009268.1:c.4002C>A	XP_016864757.1:p.Asp1334Glu
XR_001742050.2:n.4570C>A
NM_182925.5:c.4080C>A MANE Select	NP_891555.2:p.Asp1360Glu