Canonical Allele Identifier: CA362495365

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030208G>T (hg19) ; chr5:g.180603208G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603208G>T , CM000667.2:g.180603208G>T	GRCh38
NC_000005.9:g.180030208G>T , CM000667.1:g.180030208G>T	GRCh37
NC_000005.8:g.179962814G>T	NCBI36
NG_011536.1:g.51417C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4076C>A MANE Select	ENSP00000261937.6:p.Thr1359Lys
ENST00000261937.10:c.4076C>A	ENSP00000261937.6:p.Thr1359Lys
ENST00000502603.5:n.776C>A
NM_182925.4:c.4076C>A	NP_891555.2:p.Thr1359Lys
XM_011534477.1:c.4325C>A	XP_011532779.1:p.Thr1442Lys
XM_011534478.1:c.4307C>A	XP_011532780.1:p.Thr1436Lys
XM_011534482.1:c.4094C>A	XP_011532784.1:p.Thr1365Lys
XM_011534483.1:c.4016C>A	XP_011532785.1:p.Thr1339Lys
XM_011534484.1:c.3617C>A	XP_011532786.1:p.Thr1206Lys
XR_941095.1:n.4362C>A
XM_011534478.3:c.4307C>A	XP_011532780.1:p.Thr1436Lys
XM_011534484.2:c.3617C>A	XP_011532786.1:p.Thr1206Lys
XM_017009263.1:c.*222C>A	XP_016864752.1:n.*222C>A
XM_017009268.1:c.3998C>A	XP_016864757.1:p.Thr1333Lys
XR_001742050.2:n.4566C>A
NM_182925.5:c.4076C>A MANE Select	NP_891555.2:p.Thr1359Lys