Canonical Allele Identifier: CA2080983215

Gene: FLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28388529T= , CM000675.2:g.28388529T=	GRCh38
NC_000013.10:g.28962666T= , CM000675.1:g.28962666T=	GRCh37
NC_000013.9:g.27860666T=	NCBI36
NG_012003.1:g.111600A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002019.4:c.1969+1267A= MANE Select	NP_002010.2:n.1969+1267A=
ENST00000282397.9:c.1969+1267A= MANE Select	ENSP00000282397.4:n.1969+1267A=
NM_001159920.1:c.*1172A=	NP_001153392.1:n.*1172A=
NM_001159920.2:c.*1172A=	NP_001153392.1:n.*1172A=
NM_001160030.1:c.1969+1267A=	NP_001153502.1:n.1969+1267A=
NM_001160030.2:c.1969+1267A=	NP_001153502.1:n.1969+1267A=
ENST00000282397.8:c.1969+1267A=	ENSP00000282397.4:n.1969+1267A=
ENST00000541932.5:c.1969+1267A=	ENSP00000437631.1:n.1969+1267A=
ENST00000615840.4:c.*1172A=	ENSP00000484039.1:n.*1172A=
ENST00000615840.5:c.*1172A=	ENSP00000484039.1:n.*1172A=
ENST00000639477.1:c.*1075A=	ENSP00000491097.1:n.*1075A=
XM_011535014.1:c.1969+1267A=	XP_011533316.1:n.1969+1267A=
XM_017020485.1:c.1969+1267A=	XP_016875974.1:n.1969+1267A=