Canonical Allele Identifier: CA362496117

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030341A>T (hg19) ; chr5:g.180603341A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603341A>T , CM000667.2:g.180603341A>T	GRCh38
NC_000005.9:g.180030341A>T , CM000667.1:g.180030341A>T	GRCh37
NC_000005.8:g.179962947A>T	NCBI36
NG_011536.1:g.51284T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3943T>A MANE Select	ENSP00000261937.6:p.Ser1315Thr
ENST00000261937.10:c.3943T>A	ENSP00000261937.6:p.Ser1315Thr
ENST00000502603.5:n.643T>A
NM_182925.4:c.3943T>A	NP_891555.2:p.Ser1315Thr
XM_011534477.1:c.4192T>A	XP_011532779.1:p.Ser1398Thr
XM_011534478.1:c.4174T>A	XP_011532780.1:p.Ser1392Thr
XM_011534479.1:c.*89T>A	XP_011532781.1:n.*89T>A
XM_011534482.1:c.3961T>A	XP_011532784.1:p.Ser1321Thr
XM_011534483.1:c.3883T>A	XP_011532785.1:p.Ser1295Thr
XM_011534484.1:c.3484T>A	XP_011532786.1:p.Ser1162Thr
XR_941095.1:n.4229T>A
XM_011534478.3:c.4174T>A	XP_011532780.1:p.Ser1392Thr
XM_011534484.2:c.3484T>A	XP_011532786.1:p.Ser1162Thr
XM_017009263.1:c.*89T>A	XP_016864752.1:n.*89T>A
XM_017009268.1:c.3865T>A	XP_016864757.1:p.Ser1289Thr
XR_001742050.2:n.4433T>A
NM_182925.5:c.3943T>A MANE Select	NP_891555.2:p.Ser1315Thr