Canonical Allele Identifier: CA362495992

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781755
• MyVariant Identifiers: chr5:g.180030316T>C (hg19) ; chr5:g.180603316T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603316T>C , CM000667.2:g.180603316T>C	GRCh38
NC_000005.9:g.180030316T>C , CM000667.1:g.180030316T>C	GRCh37
NC_000005.8:g.179962922T>C	NCBI36
NG_011536.1:g.51309A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3968A>G MANE Select	ENSP00000261937.6:p.Glu1323Gly
ENST00000261937.10:c.3968A>G	ENSP00000261937.6:p.Glu1323Gly
ENST00000502603.5:n.668A>G
NM_182925.4:c.3968A>G	NP_891555.2:p.Glu1323Gly
XM_011534477.1:c.4217A>G	XP_011532779.1:p.Glu1406Gly
XM_011534478.1:c.4199A>G	XP_011532780.1:p.Glu1400Gly
XM_011534479.1:c.*114A>G	XP_011532781.1:n.*114A>G
XM_011534482.1:c.3986A>G	XP_011532784.1:p.Glu1329Gly
XM_011534483.1:c.3908A>G	XP_011532785.1:p.Glu1303Gly
XM_011534484.1:c.3509A>G	XP_011532786.1:p.Glu1170Gly
XR_941095.1:n.4254A>G
XM_011534478.3:c.4199A>G	XP_011532780.1:p.Glu1400Gly
XM_011534484.2:c.3509A>G	XP_011532786.1:p.Glu1170Gly
XM_017009263.1:c.*114A>G	XP_016864752.1:n.*114A>G
XM_017009268.1:c.3890A>G	XP_016864757.1:p.Glu1297Gly
XR_001742050.2:n.4458A>G
NM_182925.5:c.3968A>G MANE Select	NP_891555.2:p.Glu1323Gly