Canonical Allele Identifier: CA1604713936

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603278C= , CM000667.2:g.180603278C=	GRCh38
NC_000005.9:g.180030278C= , CM000667.1:g.180030278C=	GRCh37
NC_000005.8:g.179962884C=	NCBI36
NG_011536.1:g.51347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4006G= MANE Select	ENSP00000261937.6:p.Glu1336=
ENST00000261937.10:c.4006G=	ENSP00000261937.6:p.Glu1336=
ENST00000502603.5:n.706G=
NM_182925.4:c.4006G=	NP_891555.2:p.Glu1336=
XM_011534477.1:c.4255G=	XP_011532779.1:p.Glu1419=
XM_011534478.1:c.4237G=	XP_011532780.1:p.Glu1413=
XM_011534482.1:c.4024G=	XP_011532784.1:p.Glu1342=
XM_011534483.1:c.3946G=	XP_011532785.1:p.Glu1316=
XM_011534484.1:c.3547G=	XP_011532786.1:p.Glu1183=
XR_941095.1:n.4292G=
XM_011534478.3:c.4237G=	XP_011532780.1:p.Glu1413=
XM_011534484.2:c.3547G=	XP_011532786.1:p.Glu1183=
XM_017009263.1:c.*152G=	XP_016864752.1:n.*152G=
XM_017009268.1:c.3928G=	XP_016864757.1:p.Glu1310=
XR_001742050.2:n.4496G=
NM_182925.5:c.4006G= MANE Select	NP_891555.2:p.Glu1336=