Canonical Allele Identifier: CA362496230

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030361A>T (hg19) ; chr5:g.180603361A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603361A>T , CM000667.2:g.180603361A>T	GRCh38
NC_000005.9:g.180030361A>T , CM000667.1:g.180030361A>T	GRCh37
NC_000005.8:g.179962967A>T	NCBI36
NG_011536.1:g.51264T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3923T>A MANE Select	ENSP00000261937.6:p.Val1308Glu
ENST00000261937.10:c.3923T>A	ENSP00000261937.6:p.Val1308Glu
ENST00000502603.5:n.623T>A
NM_182925.4:c.3923T>A	NP_891555.2:p.Val1308Glu
XM_011534477.1:c.4172T>A	XP_011532779.1:p.Val1391Glu
XM_011534478.1:c.4154T>A	XP_011532780.1:p.Val1385Glu
XM_011534479.1:c.*69T>A	XP_011532781.1:n.*69T>A
XM_011534482.1:c.3941T>A	XP_011532784.1:p.Val1314Glu
XM_011534483.1:c.3863T>A	XP_011532785.1:p.Val1288Glu
XM_011534484.1:c.3464T>A	XP_011532786.1:p.Val1155Glu
XR_941095.1:n.4209T>A
XM_011534478.3:c.4154T>A	XP_011532780.1:p.Val1385Glu
XM_011534484.2:c.3464T>A	XP_011532786.1:p.Val1155Glu
XM_017009263.1:c.*69T>A	XP_016864752.1:n.*69T>A
XM_017009268.1:c.3845T>A	XP_016864757.1:p.Val1282Glu
XR_001742050.2:n.4413T>A
NM_182925.5:c.3923T>A MANE Select	NP_891555.2:p.Val1308Glu