Canonical Allele Identifier: CA362495848

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603290-A-C
• MyVariant Identifiers: chr5:g.180030290A>C (hg19) ; chr5:g.180603290A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603290A>C , CM000667.2:g.180603290A>C	GRCh38
NC_000005.9:g.180030290A>C , CM000667.1:g.180030290A>C	GRCh37
NC_000005.8:g.179962896A>C	NCBI36
NG_011536.1:g.51335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3994T>G MANE Select	ENSP00000261937.6:p.Phe1332Val
ENST00000261937.10:c.3994T>G	ENSP00000261937.6:p.Phe1332Val
ENST00000502603.5:n.694T>G
NM_182925.4:c.3994T>G	NP_891555.2:p.Phe1332Val
XM_011534477.1:c.4243T>G	XP_011532779.1:p.Phe1415Val
XM_011534478.1:c.4225T>G	XP_011532780.1:p.Phe1409Val
XM_011534482.1:c.4012T>G	XP_011532784.1:p.Phe1338Val
XM_011534483.1:c.3934T>G	XP_011532785.1:p.Phe1312Val
XM_011534484.1:c.3535T>G	XP_011532786.1:p.Phe1179Val
XR_941095.1:n.4280T>G
XM_011534478.3:c.4225T>G	XP_011532780.1:p.Phe1409Val
XM_011534484.2:c.3535T>G	XP_011532786.1:p.Phe1179Val
XM_017009263.1:c.*140T>G	XP_016864752.1:n.*140T>G
XM_017009268.1:c.3916T>G	XP_016864757.1:p.Phe1306Val
XR_001742050.2:n.4484T>G
NM_182925.5:c.3994T>G MANE Select	NP_891555.2:p.Phe1332Val