Canonical Allele Identifier: CA362495487

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030239A>T (hg19) ; chr5:g.180603239A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603239A>T , CM000667.2:g.180603239A>T	GRCh38
NC_000005.9:g.180030239A>T , CM000667.1:g.180030239A>T	GRCh37
NC_000005.8:g.179962845A>T	NCBI36
NG_011536.1:g.51386T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4045T>A MANE Select	ENSP00000261937.6:p.Cys1349Ser
ENST00000261937.10:c.4045T>A	ENSP00000261937.6:p.Cys1349Ser
ENST00000502603.5:n.745T>A
NM_182925.4:c.4045T>A	NP_891555.2:p.Cys1349Ser
XM_011534477.1:c.4294T>A	XP_011532779.1:p.Cys1432Ser
XM_011534478.1:c.4276T>A	XP_011532780.1:p.Cys1426Ser
XM_011534482.1:c.4063T>A	XP_011532784.1:p.Cys1355Ser
XM_011534483.1:c.3985T>A	XP_011532785.1:p.Cys1329Ser
XM_011534484.1:c.3586T>A	XP_011532786.1:p.Cys1196Ser
XR_941095.1:n.4331T>A
XM_011534478.3:c.4276T>A	XP_011532780.1:p.Cys1426Ser
XM_011534484.2:c.3586T>A	XP_011532786.1:p.Cys1196Ser
XM_017009263.1:c.*191T>A	XP_016864752.1:n.*191T>A
XM_017009268.1:c.3967T>A	XP_016864757.1:p.Cys1323Ser
XR_001742050.2:n.4535T>A
NM_182925.5:c.4045T>A MANE Select	NP_891555.2:p.Cys1349Ser