Canonical Allele Identifier: CA362495641

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030263A>T (hg19) ; chr5:g.180603263A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603263A>T , CM000667.2:g.180603263A>T	GRCh38
NC_000005.9:g.180030263A>T , CM000667.1:g.180030263A>T	GRCh37
NC_000005.8:g.179962869A>T	NCBI36
NG_011536.1:g.51362T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4021T>A MANE Select	ENSP00000261937.6:p.Ser1341Thr
ENST00000261937.10:c.4021T>A	ENSP00000261937.6:p.Ser1341Thr
ENST00000502603.5:n.721T>A
NM_182925.4:c.4021T>A	NP_891555.2:p.Ser1341Thr
XM_011534477.1:c.4270T>A	XP_011532779.1:p.Ser1424Thr
XM_011534478.1:c.4252T>A	XP_011532780.1:p.Ser1418Thr
XM_011534482.1:c.4039T>A	XP_011532784.1:p.Ser1347Thr
XM_011534483.1:c.3961T>A	XP_011532785.1:p.Ser1321Thr
XM_011534484.1:c.3562T>A	XP_011532786.1:p.Ser1188Thr
XR_941095.1:n.4307T>A
XM_011534478.3:c.4252T>A	XP_011532780.1:p.Ser1418Thr
XM_011534484.2:c.3562T>A	XP_011532786.1:p.Ser1188Thr
XM_017009263.1:c.*167T>A	XP_016864752.1:n.*167T>A
XM_017009268.1:c.3943T>A	XP_016864757.1:p.Ser1315Thr
XR_001742050.2:n.4511T>A
NM_182925.5:c.4021T>A MANE Select	NP_891555.2:p.Ser1341Thr