Canonical Allele Identifier: CA1604713948

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603304C= , CM000667.2:g.180603304C=	GRCh38
NC_000005.9:g.180030304C= , CM000667.1:g.180030304C=	GRCh37
NC_000005.8:g.179962910C=	NCBI36
NG_011536.1:g.51321G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3980G= MANE Select	ENSP00000261937.6:p.Arg1327=
ENST00000261937.10:c.3980G=	ENSP00000261937.6:p.Arg1327=
ENST00000502603.5:n.680G=
NM_182925.4:c.3980G=	NP_891555.2:p.Arg1327=
XM_011534477.1:c.4229G=	XP_011532779.1:p.Arg1410=
XM_011534478.1:c.4211G=	XP_011532780.1:p.Arg1404=
XM_011534479.1:c.*126G=	XP_011532781.1:n.*126G=
XM_011534482.1:c.3998G=	XP_011532784.1:p.Arg1333=
XM_011534483.1:c.3920G=	XP_011532785.1:p.Arg1307=
XM_011534484.1:c.3521G=	XP_011532786.1:p.Arg1174=
XR_941095.1:n.4266G=
XM_011534478.3:c.4211G=	XP_011532780.1:p.Arg1404=
XM_011534484.2:c.3521G=	XP_011532786.1:p.Arg1174=
XM_017009263.1:c.*126G=	XP_016864752.1:n.*126G=
XM_017009268.1:c.3902G=	XP_016864757.1:p.Arg1301=
XR_001742050.2:n.4470G=
NM_182925.5:c.3980G= MANE Select	NP_891555.2:p.Arg1327=