Canonical Allele Identifier: CA1604713901

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603224G= , CM000667.2:g.180603224G=	GRCh38
NC_000005.9:g.180030224G= , CM000667.1:g.180030224G=	GRCh37
NC_000005.8:g.179962830G=	NCBI36
NG_011536.1:g.51401C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4060C= MANE Select	ENSP00000261937.6:p.Arg1354=
ENST00000261937.10:c.4060C=	ENSP00000261937.6:p.Arg1354=
ENST00000502603.5:n.760C=
NM_182925.4:c.4060C=	NP_891555.2:p.Arg1354=
XM_011534477.1:c.4309C=	XP_011532779.1:p.Arg1437=
XM_011534478.1:c.4291C=	XP_011532780.1:p.Arg1431=
XM_011534482.1:c.4078C=	XP_011532784.1:p.Arg1360=
XM_011534483.1:c.4000C=	XP_011532785.1:p.Arg1334=
XM_011534484.1:c.3601C=	XP_011532786.1:p.Arg1201=
XR_941095.1:n.4346C=
XM_011534478.3:c.4291C=	XP_011532780.1:p.Arg1431=
XM_011534484.2:c.3601C=	XP_011532786.1:p.Arg1201=
XM_017009263.1:c.*206C=	XP_016864752.1:n.*206C=
XM_017009268.1:c.3982C=	XP_016864757.1:p.Arg1328=
XR_001742050.2:n.4550C=
NM_182925.5:c.4060C= MANE Select	NP_891555.2:p.Arg1354=