Canonical Allele Identifier: CA13827982

Gene: FLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28389565G>A , CM000675.2:g.28389565G>A	GRCh38
NC_000013.10:g.28963702G>A , CM000675.1:g.28963702G>A	GRCh37
NC_000013.9:g.27861702G>A	NCBI36
NG_012003.1:g.110564C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615840.5:c.*136C>T	ENSP00000484039.1:n.*136C>T
ENST00000282397.9:c.1969+231C>T MANE Select	ENSP00000282397.4:n.1969+231C>T
ENST00000639477.1:c.*39C>T	ENSP00000491097.1:n.*39C>T
ENST00000282397.8:c.1969+231C>T	ENSP00000282397.4:n.1969+231C>T
ENST00000541932.5:c.1969+231C>T	ENSP00000437631.1:n.1969+231C>T
ENST00000615840.4:c.*136C>T	ENSP00000484039.1:n.*136C>T
NM_001159920.1:c.*136C>T	NP_001153392.1:n.*136C>T
NM_001160030.1:c.1969+231C>T	NP_001153502.1:n.1969+231C>T
NM_002019.4:c.1969+231C>T MANE Select	NP_002010.2:n.1969+231C>T
XM_011535014.1:c.1969+231C>T	XP_011533316.1:n.1969+231C>T
XM_017020485.1:c.1969+231C>T	XP_016875974.1:n.1969+231C>T
NM_001159920.2:c.*136C>T	NP_001153392.1:n.*136C>T
NM_001160030.2:c.1969+231C>T	NP_001153502.1:n.1969+231C>T