Canonical Allele Identifier: CA448101396

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036989G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609989G>A , CM000667.2:g.180609989G>A	GRCh38
NC_000005.9:g.180036989G>A , CM000667.1:g.180036989G>A	GRCh37
NC_000005.8:g.179969595G>A	NCBI36
NG_011536.1:g.44636C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3723C>T MANE Select	ENSP00000261937.6:p.Ala1241=
ENST00000261937.10:c.3723C>T	ENSP00000261937.6:p.Ala1241=
ENST00000393347.7:c.3723C>T	ENSP00000377016.3:p.Ala1241=
ENST00000502603.5:n.423C>T
ENST00000502649.5:c.3723C>T	ENSP00000426057.1:p.Ala1241=
ENST00000507059.5:n.4073C>T
ENST00000619105.4:c.*2666C>T	ENSP00000481134.1:n.*2666C>T
NM_002020.4:c.3723C>T	NP_002011.2:p.Ala1241=
NM_182925.4:c.3723C>T	NP_891555.2:p.Ala1241=
XM_011534477.1:c.3972C>T	XP_011532779.1:p.Ala1324=
XM_011534478.1:c.3954C>T	XP_011532780.1:p.Ala1318=
XM_011534479.1:c.3972C>T	XP_011532781.1:p.Ala1324=
XM_011534480.1:c.3972C>T	XP_011532782.1:p.Ala1324=
XM_011534481.1:c.3972C>T	XP_011532783.1:p.Ala1324=
XM_011534482.1:c.3741C>T	XP_011532784.1:p.Ala1247=
XM_011534483.1:c.3663C>T	XP_011532785.1:p.Ala1221=
XM_011534484.1:c.3264C>T	XP_011532786.1:p.Ala1088=
XR_941095.1:n.4009C>T
NM_001354989.1:c.3723C>T	NP_001341918.1:p.Ala1241=
XM_011534478.3:c.3954C>T	XP_011532780.1:p.Ala1318=
XM_011534484.2:c.3264C>T	XP_011532786.1:p.Ala1088=
XM_017009263.1:c.3954C>T	XP_016864752.1:p.Ala1318=
XM_017009264.2:c.3954C>T	XP_016864753.1:p.Ala1318=
XM_017009265.1:c.3954C>T	XP_016864754.1:p.Ala1318=
XM_017009266.1:c.3954C>T	XP_016864755.1:p.Ala1318=
XM_017009267.2:c.3954C>T	XP_016864756.1:p.Ala1318=
XM_017009268.1:c.3645C>T	XP_016864757.1:p.Ala1215=
XR_001742050.2:n.4213C>T
NM_182925.5:c.3723C>T MANE Select	NP_891555.2:p.Ala1241=
NM_001354989.2:c.3723C>T	NP_001341918.1:p.Ala1241=
NM_002020.5:c.3723C>T	NP_002011.2:p.Ala1241=