Canonical Allele Identifier: CA1604713904

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603227C= , CM000667.2:g.180603227C=	GRCh38
NC_000005.9:g.180030227C= , CM000667.1:g.180030227C=	GRCh37
NC_000005.8:g.179962833C=	NCBI36
NG_011536.1:g.51398G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4057G= MANE Select	ENSP00000261937.6:p.Ala1353=
ENST00000261937.10:c.4057G=	ENSP00000261937.6:p.Ala1353=
ENST00000502603.5:n.757G=
NM_182925.4:c.4057G=	NP_891555.2:p.Ala1353=
XM_011534477.1:c.4306G=	XP_011532779.1:p.Ala1436=
XM_011534478.1:c.4288G=	XP_011532780.1:p.Ala1430=
XM_011534482.1:c.4075G=	XP_011532784.1:p.Ala1359=
XM_011534483.1:c.3997G=	XP_011532785.1:p.Ala1333=
XM_011534484.1:c.3598G=	XP_011532786.1:p.Ala1200=
XR_941095.1:n.4343G=
XM_011534478.3:c.4288G=	XP_011532780.1:p.Ala1430=
XM_011534484.2:c.3598G=	XP_011532786.1:p.Ala1200=
XM_017009263.1:c.*203G=	XP_016864752.1:n.*203G=
XM_017009268.1:c.3979G=	XP_016864757.1:p.Ala1327=
XR_001742050.2:n.4547G=
NM_182925.5:c.4057G= MANE Select	NP_891555.2:p.Ala1353=