Canonical Allele Identifier: CA362495437

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030229G>A (hg19) ; chr5:g.180603229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603229G>A , CM000667.2:g.180603229G>A	GRCh38
NC_000005.9:g.180030229G>A , CM000667.1:g.180030229G>A	GRCh37
NC_000005.8:g.179962835G>A	NCBI36
NG_011536.1:g.51396C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4055C>T MANE Select	ENSP00000261937.6:p.Ser1352Phe
ENST00000261937.10:c.4055C>T	ENSP00000261937.6:p.Ser1352Phe
ENST00000502603.5:n.755C>T
NM_182925.4:c.4055C>T	NP_891555.2:p.Ser1352Phe
XM_011534477.1:c.4304C>T	XP_011532779.1:p.Ser1435Phe
XM_011534478.1:c.4286C>T	XP_011532780.1:p.Ser1429Phe
XM_011534482.1:c.4073C>T	XP_011532784.1:p.Ser1358Phe
XM_011534483.1:c.3995C>T	XP_011532785.1:p.Ser1332Phe
XM_011534484.1:c.3596C>T	XP_011532786.1:p.Ser1199Phe
XR_941095.1:n.4341C>T
XM_011534478.3:c.4286C>T	XP_011532780.1:p.Ser1429Phe
XM_011534484.2:c.3596C>T	XP_011532786.1:p.Ser1199Phe
XM_017009263.1:c.*201C>T	XP_016864752.1:n.*201C>T
XM_017009268.1:c.3977C>T	XP_016864757.1:p.Ser1326Phe
XR_001742050.2:n.4545C>T
NM_182925.5:c.4055C>T MANE Select	NP_891555.2:p.Ser1352Phe