Canonical Allele Identifier: CA362496394

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030390G>T (hg19) ; chr5:g.180603390G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603390G>T , CM000667.2:g.180603390G>T	GRCh38
NC_000005.9:g.180030390G>T , CM000667.1:g.180030390G>T	GRCh37
NC_000005.8:g.179962996G>T	NCBI36
NG_011536.1:g.51235C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894C>A MANE Select	ENSP00000261937.6:p.Ser1298Arg
ENST00000261937.10:c.3894C>A	ENSP00000261937.6:p.Ser1298Arg
ENST00000502603.5:n.594C>A
NM_182925.4:c.3894C>A	NP_891555.2:p.Ser1298Arg
XM_011534477.1:c.4143C>A	XP_011532779.1:p.Ser1381Arg
XM_011534478.1:c.4125C>A	XP_011532780.1:p.Ser1375Arg
XM_011534479.1:c.*40C>A	XP_011532781.1:n.*40C>A
XM_011534482.1:c.3912C>A	XP_011532784.1:p.Ser1304Arg
XM_011534483.1:c.3834C>A	XP_011532785.1:p.Ser1278Arg
XM_011534484.1:c.3435C>A	XP_011532786.1:p.Ser1145Arg
XR_941095.1:n.4180C>A
XM_011534478.3:c.4125C>A	XP_011532780.1:p.Ser1375Arg
XM_011534484.2:c.3435C>A	XP_011532786.1:p.Ser1145Arg
XM_017009263.1:c.*40C>A	XP_016864752.1:n.*40C>A
XM_017009268.1:c.3816C>A	XP_016864757.1:p.Ser1272Arg
XR_001742050.2:n.4384C>A
NM_182925.5:c.3894C>A MANE Select	NP_891555.2:p.Ser1298Arg