Canonical Allele Identifier: CA448098959

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030219C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603219C>G , CM000667.2:g.180603219C>G	GRCh38
NC_000005.9:g.180030219C>G , CM000667.1:g.180030219C>G	GRCh37
NC_000005.8:g.179962825C>G	NCBI36
NG_011536.1:g.51406G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4065G>C MANE Select	ENSP00000261937.6:p.Val1355=
ENST00000261937.10:c.4065G>C	ENSP00000261937.6:p.Val1355=
ENST00000502603.5:n.765G>C
NM_182925.4:c.4065G>C	NP_891555.2:p.Val1355=
XM_011534477.1:c.4314G>C	XP_011532779.1:p.Val1438=
XM_011534478.1:c.4296G>C	XP_011532780.1:p.Val1432=
XM_011534482.1:c.4083G>C	XP_011532784.1:p.Val1361=
XM_011534483.1:c.4005G>C	XP_011532785.1:p.Val1335=
XM_011534484.1:c.3606G>C	XP_011532786.1:p.Val1202=
XR_941095.1:n.4351G>C
XM_011534478.3:c.4296G>C	XP_011532780.1:p.Val1432=
XM_011534484.2:c.3606G>C	XP_011532786.1:p.Val1202=
XM_017009263.1:c.*211G>C	XP_016864752.1:n.*211G>C
XM_017009268.1:c.3987G>C	XP_016864757.1:p.Val1329=
XR_001742050.2:n.4555G>C
NM_182925.5:c.4065G>C MANE Select	NP_891555.2:p.Val1355=