Canonical Allele Identifier: CA448099053

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781708
• MyVariant Identifiers: chr5:g.180030297G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603297G>C , CM000667.2:g.180603297G>C	GRCh38
NC_000005.9:g.180030297G>C , CM000667.1:g.180030297G>C	GRCh37
NC_000005.8:g.179962903G>C	NCBI36
NG_011536.1:g.51328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3987C>G MANE Select	ENSP00000261937.6:p.Gly1329=
ENST00000261937.10:c.3987C>G	ENSP00000261937.6:p.Gly1329=
ENST00000502603.5:n.687C>G
NM_182925.4:c.3987C>G	NP_891555.2:p.Gly1329=
XM_011534477.1:c.4236C>G	XP_011532779.1:p.Gly1412=
XM_011534478.1:c.4218C>G	XP_011532780.1:p.Gly1406=
XM_011534482.1:c.4005C>G	XP_011532784.1:p.Gly1335=
XM_011534483.1:c.3927C>G	XP_011532785.1:p.Gly1309=
XM_011534484.1:c.3528C>G	XP_011532786.1:p.Gly1176=
XR_941095.1:n.4273C>G
XM_011534478.3:c.4218C>G	XP_011532780.1:p.Gly1406=
XM_011534484.2:c.3528C>G	XP_011532786.1:p.Gly1176=
XM_017009263.1:c.*133C>G	XP_016864752.1:n.*133C>G
XM_017009268.1:c.3909C>G	XP_016864757.1:p.Gly1303=
XR_001742050.2:n.4477C>G
NM_182925.5:c.3987C>G MANE Select	NP_891555.2:p.Gly1329=