Canonical Allele Identifier: CA362496089

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030337T>C (hg19) ; chr5:g.180603337T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603337T>C , CM000667.2:g.180603337T>C	GRCh38
NC_000005.9:g.180030337T>C , CM000667.1:g.180030337T>C	GRCh37
NC_000005.8:g.179962943T>C	NCBI36
NG_011536.1:g.51288A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3947A>G MANE Select	ENSP00000261937.6:p.Gln1316Arg
ENST00000261937.10:c.3947A>G	ENSP00000261937.6:p.Gln1316Arg
ENST00000502603.5:n.647A>G
NM_182925.4:c.3947A>G	NP_891555.2:p.Gln1316Arg
XM_011534477.1:c.4196A>G	XP_011532779.1:p.Gln1399Arg
XM_011534478.1:c.4178A>G	XP_011532780.1:p.Gln1393Arg
XM_011534479.1:c.*93A>G	XP_011532781.1:n.*93A>G
XM_011534482.1:c.3965A>G	XP_011532784.1:p.Gln1322Arg
XM_011534483.1:c.3887A>G	XP_011532785.1:p.Gln1296Arg
XM_011534484.1:c.3488A>G	XP_011532786.1:p.Gln1163Arg
XR_941095.1:n.4233A>G
XM_011534478.3:c.4178A>G	XP_011532780.1:p.Gln1393Arg
XM_011534484.2:c.3488A>G	XP_011532786.1:p.Gln1163Arg
XM_017009263.1:c.*93A>G	XP_016864752.1:n.*93A>G
XM_017009268.1:c.3869A>G	XP_016864757.1:p.Gln1290Arg
XR_001742050.2:n.4437A>G
NM_182925.5:c.3947A>G MANE Select	NP_891555.2:p.Gln1316Arg