Canonical Allele Identifier: CA1604713878

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603173G= , CM000667.2:g.180603173G=	GRCh38
NC_000005.9:g.180030173G= , CM000667.1:g.180030173G=	GRCh37
NC_000005.8:g.179962779G=	NCBI36
NG_011536.1:g.51452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*19C= MANE Select	ENSP00000261937.6:n.*19C=
ENST00000261937.10:c.*19C=	ENSP00000261937.6:n.*19C=
ENST00000502603.5:n.811C=
NM_182925.4:c.*19C=	NP_891555.2:n.*19C=
XM_011534477.1:c.*19C=	XP_011532779.1:n.*19C=
XM_011534478.1:c.*19C=	XP_011532780.1:n.*19C=
XM_011534482.1:c.*19C=	XP_011532784.1:n.*19C=
XM_011534483.1:c.*19C=	XP_011532785.1:n.*19C=
XM_011534484.1:c.*19C=	XP_011532786.1:n.*19C=
XR_941095.1:n.4397C=
XM_011534478.3:c.*19C=	XP_011532780.1:n.*19C=
XM_011534484.2:c.*19C=	XP_011532786.1:n.*19C=
XM_017009263.1:c.*257C=	XP_016864752.1:n.*257C=
XM_017009268.1:c.*19C=	XP_016864757.1:n.*19C=
XR_001742050.2:n.4601C=
NM_182925.5:c.*19C= MANE Select	NP_891555.2:n.*19C=