Canonical Allele Identifier: CA1604713956

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603313C= , CM000667.2:g.180603313C=	GRCh38
NC_000005.9:g.180030313C= , CM000667.1:g.180030313C=	GRCh37
NC_000005.8:g.179962919C=	NCBI36
NG_011536.1:g.51312G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3971G= MANE Select	ENSP00000261937.6:p.Arg1324=
ENST00000261937.10:c.3971G=	ENSP00000261937.6:p.Arg1324=
ENST00000502603.5:n.671G=
NM_182925.4:c.3971G=	NP_891555.2:p.Arg1324=
XM_011534477.1:c.4220G=	XP_011532779.1:p.Arg1407=
XM_011534478.1:c.4202G=	XP_011532780.1:p.Arg1401=
XM_011534479.1:c.*117G=	XP_011532781.1:n.*117G=
XM_011534482.1:c.3989G=	XP_011532784.1:p.Arg1330=
XM_011534483.1:c.3911G=	XP_011532785.1:p.Arg1304=
XM_011534484.1:c.3512G=	XP_011532786.1:p.Arg1171=
XR_941095.1:n.4257G=
XM_011534478.3:c.4202G=	XP_011532780.1:p.Arg1401=
XM_011534484.2:c.3512G=	XP_011532786.1:p.Arg1171=
XM_017009263.1:c.*117G=	XP_016864752.1:n.*117G=
XM_017009268.1:c.3893G=	XP_016864757.1:p.Arg1298=
XR_001742050.2:n.4461G=
NM_182925.5:c.3971G= MANE Select	NP_891555.2:p.Arg1324=