Canonical Allele Identifier: CA362496364

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030385T>C (hg19) ; chr5:g.180603385T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603385T>C , CM000667.2:g.180603385T>C	GRCh38
NC_000005.9:g.180030385T>C , CM000667.1:g.180030385T>C	GRCh37
NC_000005.8:g.179962991T>C	NCBI36
NG_011536.1:g.51240A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3899A>G MANE Select	ENSP00000261937.6:p.Lys1300Arg
ENST00000261937.10:c.3899A>G	ENSP00000261937.6:p.Lys1300Arg
ENST00000502603.5:n.599A>G
NM_182925.4:c.3899A>G	NP_891555.2:p.Lys1300Arg
XM_011534477.1:c.4148A>G	XP_011532779.1:p.Lys1383Arg
XM_011534478.1:c.4130A>G	XP_011532780.1:p.Lys1377Arg
XM_011534479.1:c.*45A>G	XP_011532781.1:n.*45A>G
XM_011534482.1:c.3917A>G	XP_011532784.1:p.Lys1306Arg
XM_011534483.1:c.3839A>G	XP_011532785.1:p.Lys1280Arg
XM_011534484.1:c.3440A>G	XP_011532786.1:p.Lys1147Arg
XR_941095.1:n.4185A>G
XM_011534478.3:c.4130A>G	XP_011532780.1:p.Lys1377Arg
XM_011534484.2:c.3440A>G	XP_011532786.1:p.Lys1147Arg
XM_017009263.1:c.*45A>G	XP_016864752.1:n.*45A>G
XM_017009268.1:c.3821A>G	XP_016864757.1:p.Lys1274Arg
XR_001742050.2:n.4389A>G
NM_182925.5:c.3899A>G MANE Select	NP_891555.2:p.Lys1300Arg