Canonical Allele Identifier: CA362496332

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030379G>T (hg19) ; chr5:g.180603379G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603379G>T , CM000667.2:g.180603379G>T	GRCh38
NC_000005.9:g.180030379G>T , CM000667.1:g.180030379G>T	GRCh37
NC_000005.8:g.179962985G>T	NCBI36
NG_011536.1:g.51246C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3905C>A MANE Select	ENSP00000261937.6:p.Pro1302His
ENST00000261937.10:c.3905C>A	ENSP00000261937.6:p.Pro1302His
ENST00000502603.5:n.605C>A
NM_182925.4:c.3905C>A	NP_891555.2:p.Pro1302His
XM_011534477.1:c.4154C>A	XP_011532779.1:p.Pro1385His
XM_011534478.1:c.4136C>A	XP_011532780.1:p.Pro1379His
XM_011534479.1:c.*51C>A	XP_011532781.1:n.*51C>A
XM_011534482.1:c.3923C>A	XP_011532784.1:p.Pro1308His
XM_011534483.1:c.3845C>A	XP_011532785.1:p.Pro1282His
XM_011534484.1:c.3446C>A	XP_011532786.1:p.Pro1149His
XR_941095.1:n.4191C>A
XM_011534478.3:c.4136C>A	XP_011532780.1:p.Pro1379His
XM_011534484.2:c.3446C>A	XP_011532786.1:p.Pro1149His
XM_017009263.1:c.*51C>A	XP_016864752.1:n.*51C>A
XM_017009268.1:c.3827C>A	XP_016864757.1:p.Pro1276His
XR_001742050.2:n.4395C>A
NM_182925.5:c.3905C>A MANE Select	NP_891555.2:p.Pro1302His