Canonical Allele Identifier: CA1604713921

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603249C= , CM000667.2:g.180603249C=	GRCh38
NC_000005.9:g.180030249C= , CM000667.1:g.180030249C=	GRCh37
NC_000005.8:g.179962855C=	NCBI36
NG_011536.1:g.51376G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4035G= MANE Select	ENSP00000261937.6:p.Glu1345=
ENST00000261937.10:c.4035G=	ENSP00000261937.6:p.Glu1345=
ENST00000502603.5:n.735G=
NM_182925.4:c.4035G=	NP_891555.2:p.Glu1345=
XM_011534477.1:c.4284G=	XP_011532779.1:p.Glu1428=
XM_011534478.1:c.4266G=	XP_011532780.1:p.Glu1422=
XM_011534482.1:c.4053G=	XP_011532784.1:p.Glu1351=
XM_011534483.1:c.3975G=	XP_011532785.1:p.Glu1325=
XM_011534484.1:c.3576G=	XP_011532786.1:p.Glu1192=
XR_941095.1:n.4321G=
XM_011534478.3:c.4266G=	XP_011532780.1:p.Glu1422=
XM_011534484.2:c.3576G=	XP_011532786.1:p.Glu1192=
XM_017009263.1:c.*181G=	XP_016864752.1:n.*181G=
XM_017009268.1:c.3957G=	XP_016864757.1:p.Glu1319=
XR_001742050.2:n.4525G=
NM_182925.5:c.4035G= MANE Select	NP_891555.2:p.Glu1345=