Canonical Allele Identifier: CA448099086

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030332T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603332T>G , CM000667.2:g.180603332T>G	GRCh38
NC_000005.9:g.180030332T>G , CM000667.1:g.180030332T>G	GRCh37
NC_000005.8:g.179962938T>G	NCBI36
NG_011536.1:g.51293A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3952A>C MANE Select	ENSP00000261937.6:p.Arg1318=
ENST00000261937.10:c.3952A>C	ENSP00000261937.6:p.Arg1318=
ENST00000502603.5:n.652A>C
NM_182925.4:c.3952A>C	NP_891555.2:p.Arg1318=
XM_011534477.1:c.4201A>C	XP_011532779.1:p.Arg1401=
XM_011534478.1:c.4183A>C	XP_011532780.1:p.Arg1395=
XM_011534479.1:c.*98A>C	XP_011532781.1:n.*98A>C
XM_011534482.1:c.3970A>C	XP_011532784.1:p.Arg1324=
XM_011534483.1:c.3892A>C	XP_011532785.1:p.Arg1298=
XM_011534484.1:c.3493A>C	XP_011532786.1:p.Arg1165=
XR_941095.1:n.4238A>C
XM_011534478.3:c.4183A>C	XP_011532780.1:p.Arg1395=
XM_011534484.2:c.3493A>C	XP_011532786.1:p.Arg1165=
XM_017009263.1:c.*98A>C	XP_016864752.1:n.*98A>C
XM_017009268.1:c.3874A>C	XP_016864757.1:p.Arg1292=
XR_001742050.2:n.4442A>C
NM_182925.5:c.3952A>C MANE Select	NP_891555.2:p.Arg1318=