Canonical Allele Identifier: CA362495794

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781695
• COSMIC: COSM3614869
• MyVariant Identifiers: chr5:g.180030280C>T (hg19) ; chr5:g.180603280C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603280C>T , CM000667.2:g.180603280C>T	GRCh38
NC_000005.9:g.180030280C>T , CM000667.1:g.180030280C>T	GRCh37
NC_000005.8:g.179962886C>T	NCBI36
NG_011536.1:g.51345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4004G>A MANE Select	ENSP00000261937.6:p.Ser1335Asn
ENST00000261937.10:c.4004G>A	ENSP00000261937.6:p.Ser1335Asn
ENST00000502603.5:n.704G>A
NM_182925.4:c.4004G>A	NP_891555.2:p.Ser1335Asn
XM_011534477.1:c.4253G>A	XP_011532779.1:p.Ser1418Asn
XM_011534478.1:c.4235G>A	XP_011532780.1:p.Ser1412Asn
XM_011534482.1:c.4022G>A	XP_011532784.1:p.Ser1341Asn
XM_011534483.1:c.3944G>A	XP_011532785.1:p.Ser1315Asn
XM_011534484.1:c.3545G>A	XP_011532786.1:p.Ser1182Asn
XR_941095.1:n.4290G>A
XM_011534478.3:c.4235G>A	XP_011532780.1:p.Ser1412Asn
XM_011534484.2:c.3545G>A	XP_011532786.1:p.Ser1182Asn
XM_017009263.1:c.*150G>A	XP_016864752.1:n.*150G>A
XM_017009268.1:c.3926G>A	XP_016864757.1:p.Ser1309Asn
XR_001742050.2:n.4494G>A
NM_182925.5:c.4004G>A MANE Select	NP_891555.2:p.Ser1335Asn