Canonical Allele Identifier: CA1604713963

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603323G= , CM000667.2:g.180603323G=	GRCh38
NC_000005.9:g.180030323G= , CM000667.1:g.180030323G=	GRCh37
NC_000005.8:g.179962929G=	NCBI36
NG_011536.1:g.51302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3961C= MANE Select	ENSP00000261937.6:p.Arg1321=
ENST00000261937.10:c.3961C=	ENSP00000261937.6:p.Arg1321=
ENST00000502603.5:n.661C=
NM_182925.4:c.3961C=	NP_891555.2:p.Arg1321=
XM_011534477.1:c.4210C=	XP_011532779.1:p.Arg1404=
XM_011534478.1:c.4192C=	XP_011532780.1:p.Arg1398=
XM_011534479.1:c.*107C=	XP_011532781.1:n.*107C=
XM_011534482.1:c.3979C=	XP_011532784.1:p.Arg1327=
XM_011534483.1:c.3901C=	XP_011532785.1:p.Arg1301=
XM_011534484.1:c.3502C=	XP_011532786.1:p.Arg1168=
XR_941095.1:n.4247C=
XM_011534478.3:c.4192C=	XP_011532780.1:p.Arg1398=
XM_011534484.2:c.3502C=	XP_011532786.1:p.Arg1168=
XM_017009263.1:c.*107C=	XP_016864752.1:n.*107C=
XM_017009268.1:c.3883C=	XP_016864757.1:p.Arg1295=
XR_001742050.2:n.4451C=
NM_182925.5:c.3961C= MANE Select	NP_891555.2:p.Arg1321=