Canonical Allele Identifier: CA362495897

Gene: FLT4

Linked Data

• dbSNP Id: rs1581596674
• MyVariant Identifiers: chr5:g.180030295T>C (hg19) ; chr5:g.180603295T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603295T>C , CM000667.2:g.180603295T>C	GRCh38
NC_000005.9:g.180030295T>C , CM000667.1:g.180030295T>C	GRCh37
NC_000005.8:g.179962901T>C	NCBI36
NG_011536.1:g.51330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3989A>G MANE Select	ENSP00000261937.6:p.Gln1330Arg
ENST00000261937.10:c.3989A>G	ENSP00000261937.6:p.Gln1330Arg
ENST00000502603.5:n.689A>G
NM_182925.4:c.3989A>G	NP_891555.2:p.Gln1330Arg
XM_011534477.1:c.4238A>G	XP_011532779.1:p.Gln1413Arg
XM_011534478.1:c.4220A>G	XP_011532780.1:p.Gln1407Arg
XM_011534482.1:c.4007A>G	XP_011532784.1:p.Gln1336Arg
XM_011534483.1:c.3929A>G	XP_011532785.1:p.Gln1310Arg
XM_011534484.1:c.3530A>G	XP_011532786.1:p.Gln1177Arg
XR_941095.1:n.4275A>G
XM_011534478.3:c.4220A>G	XP_011532780.1:p.Gln1407Arg
XM_011534484.2:c.3530A>G	XP_011532786.1:p.Gln1177Arg
XM_017009263.1:c.*135A>G	XP_016864752.1:n.*135A>G
XM_017009268.1:c.3911A>G	XP_016864757.1:p.Gln1304Arg
XR_001742050.2:n.4479A>G
NM_182925.5:c.3989A>G MANE Select	NP_891555.2:p.Gln1330Arg