Canonical Allele Identifier: CA362495326

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030194A>T (hg19) ; chr5:g.180603194A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603194A>T , CM000667.2:g.180603194A>T	GRCh38
NC_000005.9:g.180030194A>T , CM000667.1:g.180030194A>T	GRCh37
NC_000005.8:g.179962800A>T	NCBI36
NG_011536.1:g.51431T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4090T>A MANE Select	ENSP00000261937.6:p.Ter1364Lys
ENST00000261937.10:c.4090T>A	ENSP00000261937.6:p.Ter1364Lys
ENST00000502603.5:n.790T>A
NM_182925.4:c.4090T>A	NP_891555.2:p.Ter1364Lys
XM_011534477.1:c.4339T>A	XP_011532779.1:p.Ter1447Lys
XM_011534478.1:c.4321T>A	XP_011532780.1:p.Ter1441Lys
XM_011534482.1:c.4108T>A	XP_011532784.1:p.Ter1370Lys
XM_011534483.1:c.4030T>A	XP_011532785.1:p.Ter1344Lys
XM_011534484.1:c.3631T>A	XP_011532786.1:p.Ter1211Lys
XR_941095.1:n.4376T>A
XM_011534478.3:c.4321T>A	XP_011532780.1:p.Ter1441Lys
XM_011534484.2:c.3631T>A	XP_011532786.1:p.Ter1211Lys
XM_017009263.1:c.*236T>A	XP_016864752.1:n.*236T>A
XM_017009268.1:c.4012T>A	XP_016864757.1:p.Ter1338Lys
XR_001742050.2:n.4580T>A
NM_182925.5:c.4090T>A MANE Select	NP_891555.2:p.Ter1364Lys