Canonical Allele Identifier: CA362498089

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180037009A>T (hg19) ; chr5:g.180610009A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180610009A>T , CM000667.2:g.180610009A>T	GRCh38
NC_000005.9:g.180037009A>T , CM000667.1:g.180037009A>T	GRCh37
NC_000005.8:g.179969615A>T	NCBI36
NG_011536.1:g.44616T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3703T>A MANE Select	ENSP00000261937.6:p.Ser1235Thr
ENST00000261937.10:c.3703T>A	ENSP00000261937.6:p.Ser1235Thr
ENST00000393347.7:c.3703T>A	ENSP00000377016.3:p.Ser1235Thr
ENST00000502603.5:n.403T>A
ENST00000502649.5:c.3703T>A	ENSP00000426057.1:p.Ser1235Thr
ENST00000507059.5:n.4053T>A
ENST00000619105.4:c.*2646T>A	ENSP00000481134.1:n.*2646T>A
NM_002020.4:c.3703T>A	NP_002011.2:p.Ser1235Thr
NM_182925.4:c.3703T>A	NP_891555.2:p.Ser1235Thr
XM_011534477.1:c.3952T>A	XP_011532779.1:p.Ser1318Thr
XM_011534478.1:c.3934T>A	XP_011532780.1:p.Ser1312Thr
XM_011534479.1:c.3952T>A	XP_011532781.1:p.Ser1318Thr
XM_011534480.1:c.3952T>A	XP_011532782.1:p.Ser1318Thr
XM_011534481.1:c.3952T>A	XP_011532783.1:p.Ser1318Thr
XM_011534482.1:c.3721T>A	XP_011532784.1:p.Ser1241Thr
XM_011534483.1:c.3643T>A	XP_011532785.1:p.Ser1215Thr
XM_011534484.1:c.3244T>A	XP_011532786.1:p.Ser1082Thr
XR_941095.1:n.3989T>A
NM_001354989.1:c.3703T>A	NP_001341918.1:p.Ser1235Thr
XM_011534478.3:c.3934T>A	XP_011532780.1:p.Ser1312Thr
XM_011534484.2:c.3244T>A	XP_011532786.1:p.Ser1082Thr
XM_017009263.1:c.3934T>A	XP_016864752.1:p.Ser1312Thr
XM_017009264.2:c.3934T>A	XP_016864753.1:p.Ser1312Thr
XM_017009265.1:c.3934T>A	XP_016864754.1:p.Ser1312Thr
XM_017009266.1:c.3934T>A	XP_016864755.1:p.Ser1312Thr
XM_017009267.2:c.3934T>A	XP_016864756.1:p.Ser1312Thr
XM_017009268.1:c.3625T>A	XP_016864757.1:p.Ser1209Thr
XR_001742050.2:n.4193T>A
NM_182925.5:c.3703T>A MANE Select	NP_891555.2:p.Ser1235Thr
NM_001354989.2:c.3703T>A	NP_001341918.1:p.Ser1235Thr
NM_002020.5:c.3703T>A	NP_002011.2:p.Ser1235Thr