Canonical Allele Identifier: CA362495346

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030200T>A (hg19) ; chr5:g.180603200T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603200T>A , CM000667.2:g.180603200T>A	GRCh38
NC_000005.9:g.180030200T>A , CM000667.1:g.180030200T>A	GRCh37
NC_000005.8:g.179962806T>A	NCBI36
NG_011536.1:g.51425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4084A>T MANE Select	ENSP00000261937.6:p.Ser1362Cys
ENST00000261937.10:c.4084A>T	ENSP00000261937.6:p.Ser1362Cys
ENST00000502603.5:n.784A>T
NM_182925.4:c.4084A>T	NP_891555.2:p.Ser1362Cys
XM_011534477.1:c.4333A>T	XP_011532779.1:p.Ser1445Cys
XM_011534478.1:c.4315A>T	XP_011532780.1:p.Ser1439Cys
XM_011534482.1:c.4102A>T	XP_011532784.1:p.Ser1368Cys
XM_011534483.1:c.4024A>T	XP_011532785.1:p.Ser1342Cys
XM_011534484.1:c.3625A>T	XP_011532786.1:p.Ser1209Cys
XR_941095.1:n.4370A>T
XM_011534478.3:c.4315A>T	XP_011532780.1:p.Ser1439Cys
XM_011534484.2:c.3625A>T	XP_011532786.1:p.Ser1209Cys
XM_017009263.1:c.*230A>T	XP_016864752.1:n.*230A>T
XM_017009268.1:c.4006A>T	XP_016864757.1:p.Ser1336Cys
XR_001742050.2:n.4574A>T
NM_182925.5:c.4084A>T MANE Select	NP_891555.2:p.Ser1362Cys