Canonical Allele Identifier: CA1604713899

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603222G= , CM000667.2:g.180603222G=	GRCh38
NC_000005.9:g.180030222G= , CM000667.1:g.180030222G=	GRCh37
NC_000005.8:g.179962828G=	NCBI36
NG_011536.1:g.51403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4062C= MANE Select	ENSP00000261937.6:p.Arg1354=
ENST00000261937.10:c.4062C=	ENSP00000261937.6:p.Arg1354=
ENST00000502603.5:n.762C=
NM_182925.4:c.4062C=	NP_891555.2:p.Arg1354=
XM_011534477.1:c.4311C=	XP_011532779.1:p.Arg1437=
XM_011534478.1:c.4293C=	XP_011532780.1:p.Arg1431=
XM_011534482.1:c.4080C=	XP_011532784.1:p.Arg1360=
XM_011534483.1:c.4002C=	XP_011532785.1:p.Arg1334=
XM_011534484.1:c.3603C=	XP_011532786.1:p.Arg1201=
XR_941095.1:n.4348C=
XM_011534478.3:c.4293C=	XP_011532780.1:p.Arg1431=
XM_011534484.2:c.3603C=	XP_011532786.1:p.Arg1201=
XM_017009263.1:c.*208C=	XP_016864752.1:n.*208C=
XM_017009268.1:c.3984C=	XP_016864757.1:p.Arg1328=
XR_001742050.2:n.4552C=
NM_182925.5:c.4062C= MANE Select	NP_891555.2:p.Arg1354=