Canonical Allele Identifier: CA362495517

Gene: FLT4

Linked Data

• dbSNP Id: rs1761605234
• MyVariant Identifiers: chr5:g.180030245C>T (hg19) ; chr5:g.180603245C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603245C>T , CM000667.2:g.180603245C>T	GRCh38
NC_000005.9:g.180030245C>T , CM000667.1:g.180030245C>T	GRCh37
NC_000005.8:g.179962851C>T	NCBI36
NG_011536.1:g.51380G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4039G>A MANE Select	ENSP00000261937.6:p.Asp1347Asn
ENST00000261937.10:c.4039G>A	ENSP00000261937.6:p.Asp1347Asn
ENST00000502603.5:n.739G>A
NM_182925.4:c.4039G>A	NP_891555.2:p.Asp1347Asn
XM_011534477.1:c.4288G>A	XP_011532779.1:p.Asp1430Asn
XM_011534478.1:c.4270G>A	XP_011532780.1:p.Asp1424Asn
XM_011534482.1:c.4057G>A	XP_011532784.1:p.Asp1353Asn
XM_011534483.1:c.3979G>A	XP_011532785.1:p.Asp1327Asn
XM_011534484.1:c.3580G>A	XP_011532786.1:p.Asp1194Asn
XR_941095.1:n.4325G>A
XM_011534478.3:c.4270G>A	XP_011532780.1:p.Asp1424Asn
XM_011534484.2:c.3580G>A	XP_011532786.1:p.Asp1194Asn
XM_017009263.1:c.*185G>A	XP_016864752.1:n.*185G>A
XM_017009268.1:c.3961G>A	XP_016864757.1:p.Asp1321Asn
XR_001742050.2:n.4529G>A
NM_182925.5:c.4039G>A MANE Select	NP_891555.2:p.Asp1347Asn