Canonical Allele Identifier: CA1604713507

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602479C= , CM000667.2:g.180602479C=	GRCh38
NC_000005.9:g.180029479C= , CM000667.1:g.180029479C=	GRCh37
NC_000005.8:g.179962085C=	NCBI36
NG_011536.1:g.52146G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.*713G= MANE Select	ENSP00000261937.6:n.*713G=
ENST00000261937.10:c.*713G=	ENSP00000261937.6:n.*713G=
NM_182925.4:c.*713G=	NP_891555.2:n.*713G=
XM_011534477.1:c.*713G=	XP_011532779.1:n.*713G=
XM_011534478.1:c.*713G=	XP_011532780.1:n.*713G=
XM_011534482.1:c.*713G=	XP_011532784.1:n.*713G=
XM_011534483.1:c.*713G=	XP_011532785.1:n.*713G=
XM_011534484.1:c.*713G=	XP_011532786.1:n.*713G=
XM_011534478.3:c.*713G=	XP_011532780.1:n.*713G=
XM_011534484.2:c.*713G=	XP_011532786.1:n.*713G=
XM_017009263.1:c.*951G=	XP_016864752.1:n.*951G=
XM_017009268.1:c.*713G=	XP_016864757.1:n.*713G=
XR_001742050.2:n.5295G=
NM_182925.5:c.*713G= MANE Select	NP_891555.2:n.*713G=