Canonical Allele Identifier: CA362496125

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030343T>A (hg19) ; chr5:g.180603343T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603343T>A , CM000667.2:g.180603343T>A	GRCh38
NC_000005.9:g.180030343T>A , CM000667.1:g.180030343T>A	GRCh37
NC_000005.8:g.179962949T>A	NCBI36
NG_011536.1:g.51282A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3941A>T MANE Select	ENSP00000261937.6:p.Asp1314Val
ENST00000261937.10:c.3941A>T	ENSP00000261937.6:p.Asp1314Val
ENST00000502603.5:n.641A>T
NM_182925.4:c.3941A>T	NP_891555.2:p.Asp1314Val
XM_011534477.1:c.4190A>T	XP_011532779.1:p.Asp1397Val
XM_011534478.1:c.4172A>T	XP_011532780.1:p.Asp1391Val
XM_011534479.1:c.*87A>T	XP_011532781.1:n.*87A>T
XM_011534482.1:c.3959A>T	XP_011532784.1:p.Asp1320Val
XM_011534483.1:c.3881A>T	XP_011532785.1:p.Asp1294Val
XM_011534484.1:c.3482A>T	XP_011532786.1:p.Asp1161Val
XR_941095.1:n.4227A>T
XM_011534478.3:c.4172A>T	XP_011532780.1:p.Asp1391Val
XM_011534484.2:c.3482A>T	XP_011532786.1:p.Asp1161Val
XM_017009263.1:c.*87A>T	XP_016864752.1:n.*87A>T
XM_017009268.1:c.3863A>T	XP_016864757.1:p.Asp1288Val
XR_001742050.2:n.4431A>T
NM_182925.5:c.3941A>T MANE Select	NP_891555.2:p.Asp1314Val