Canonical Allele Identifier: CA448101386

Gene: FLT4

Linked Data

• dbSNP Id: rs2127788845
• MyVariant Identifiers: chr5:g.180036980A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609980A>G , CM000667.2:g.180609980A>G	GRCh38
NC_000005.9:g.180036980A>G , CM000667.1:g.180036980A>G	GRCh37
NC_000005.8:g.179969586A>G	NCBI36
NG_011536.1:g.44645T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3732T>C MANE Select	ENSP00000261937.6:p.Ala1244=
ENST00000261937.10:c.3732T>C	ENSP00000261937.6:p.Ala1244=
ENST00000393347.7:c.3732T>C	ENSP00000377016.3:p.Ala1244=
ENST00000502603.5:n.432T>C
ENST00000502649.5:c.3732T>C	ENSP00000426057.1:p.Ala1244=
ENST00000507059.5:n.4082T>C
ENST00000619105.4:c.*2675T>C	ENSP00000481134.1:n.*2675T>C
NM_002020.4:c.3732T>C	NP_002011.2:p.Ala1244=
NM_182925.4:c.3732T>C	NP_891555.2:p.Ala1244=
XM_011534477.1:c.3981T>C	XP_011532779.1:p.Ala1327=
XM_011534478.1:c.3963T>C	XP_011532780.1:p.Ala1321=
XM_011534479.1:c.3981T>C	XP_011532781.1:p.Ala1327=
XM_011534480.1:c.3981T>C	XP_011532782.1:p.Ala1327=
XM_011534481.1:c.3981T>C	XP_011532783.1:p.Ala1327=
XM_011534482.1:c.3750T>C	XP_011532784.1:p.Ala1250=
XM_011534483.1:c.3672T>C	XP_011532785.1:p.Ala1224=
XM_011534484.1:c.3273T>C	XP_011532786.1:p.Ala1091=
XR_941095.1:n.4018T>C
NM_001354989.1:c.3732T>C	NP_001341918.1:p.Ala1244=
XM_011534478.3:c.3963T>C	XP_011532780.1:p.Ala1321=
XM_011534484.2:c.3273T>C	XP_011532786.1:p.Ala1091=
XM_017009263.1:c.3963T>C	XP_016864752.1:p.Ala1321=
XM_017009264.2:c.3963T>C	XP_016864753.1:p.Ala1321=
XM_017009265.1:c.3963T>C	XP_016864754.1:p.Ala1321=
XM_017009266.1:c.3963T>C	XP_016864755.1:p.Ala1321=
XM_017009267.2:c.3963T>C	XP_016864756.1:p.Ala1321=
XM_017009268.1:c.3654T>C	XP_016864757.1:p.Ala1218=
XR_001742050.2:n.4222T>C
NM_182925.5:c.3732T>C MANE Select	NP_891555.2:p.Ala1244=
NM_001354989.2:c.3732T>C	NP_001341918.1:p.Ala1244=
NM_002020.5:c.3732T>C	NP_002011.2:p.Ala1244=