Canonical Allele Identifier: CA2080983217

Gene: FLT1

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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