Canonical Allele Identifier: CA448099011

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781627
• gnomAD v4: 5-180603237-G-A
• MyVariant Identifiers: chr5:g.180030237G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603237G>A , CM000667.2:g.180603237G>A	GRCh38
NC_000005.9:g.180030237G>A , CM000667.1:g.180030237G>A	GRCh37
NC_000005.8:g.179962843G>A	NCBI36
NG_011536.1:g.51388C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4047C>T MANE Select	ENSP00000261937.6:p.Cys1349=
ENST00000261937.10:c.4047C>T	ENSP00000261937.6:p.Cys1349=
ENST00000502603.5:n.747C>T
NM_182925.4:c.4047C>T	NP_891555.2:p.Cys1349=
XM_011534477.1:c.4296C>T	XP_011532779.1:p.Cys1432=
XM_011534478.1:c.4278C>T	XP_011532780.1:p.Cys1426=
XM_011534482.1:c.4065C>T	XP_011532784.1:p.Cys1355=
XM_011534483.1:c.3987C>T	XP_011532785.1:p.Cys1329=
XM_011534484.1:c.3588C>T	XP_011532786.1:p.Cys1196=
XR_941095.1:n.4333C>T
XM_011534478.3:c.4278C>T	XP_011532780.1:p.Cys1426=
XM_011534484.2:c.3588C>T	XP_011532786.1:p.Cys1196=
XM_017009263.1:c.*193C>T	XP_016864752.1:n.*193C>T
XM_017009268.1:c.3969C>T	XP_016864757.1:p.Cys1323=
XR_001742050.2:n.4537C>T
NM_182925.5:c.4047C>T MANE Select	NP_891555.2:p.Cys1349=