Canonical Allele Identifier: CA362495836

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030288A>C (hg19) ; chr5:g.180603288A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603288A>C , CM000667.2:g.180603288A>C	GRCh38
NC_000005.9:g.180030288A>C , CM000667.1:g.180030288A>C	GRCh37
NC_000005.8:g.179962894A>C	NCBI36
NG_011536.1:g.51337T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3996T>G MANE Select	ENSP00000261937.6:p.Phe1332Leu
ENST00000261937.10:c.3996T>G	ENSP00000261937.6:p.Phe1332Leu
ENST00000502603.5:n.696T>G
NM_182925.4:c.3996T>G	NP_891555.2:p.Phe1332Leu
XM_011534477.1:c.4245T>G	XP_011532779.1:p.Phe1415Leu
XM_011534478.1:c.4227T>G	XP_011532780.1:p.Phe1409Leu
XM_011534482.1:c.4014T>G	XP_011532784.1:p.Phe1338Leu
XM_011534483.1:c.3936T>G	XP_011532785.1:p.Phe1312Leu
XM_011534484.1:c.3537T>G	XP_011532786.1:p.Phe1179Leu
XR_941095.1:n.4282T>G
XM_011534478.3:c.4227T>G	XP_011532780.1:p.Phe1409Leu
XM_011534484.2:c.3537T>G	XP_011532786.1:p.Phe1179Leu
XM_017009263.1:c.*142T>G	XP_016864752.1:n.*142T>G
XM_017009268.1:c.3918T>G	XP_016864757.1:p.Phe1306Leu
XR_001742050.2:n.4486T>G
NM_182925.5:c.3996T>G MANE Select	NP_891555.2:p.Phe1332Leu