Canonical Allele Identifier: CA2080983867

Gene: FLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28390188G= , CM000675.2:g.28390188G=	GRCh38
NC_000013.10:g.28964325G= , CM000675.1:g.28964325G=	GRCh37
NC_000013.9:g.27862325G=	NCBI36
NG_012003.1:g.109941C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002019.4:c.1661-84C= MANE Select	NP_002010.2:n.1661-84C=
ENST00000282397.9:c.1661-84C= MANE Select	ENSP00000282397.4:n.1661-84C=
NM_001159920.1:c.1661-84C=	NP_001153392.1:n.1661-84C=
NM_001159920.2:c.1661-84C=	NP_001153392.1:n.1661-84C=
NM_001160030.1:c.1661-84C=	NP_001153502.1:n.1661-84C=
NM_001160030.2:c.1661-84C=	NP_001153502.1:n.1661-84C=
ENST00000282397.8:c.1661-84C=	ENSP00000282397.4:n.1661-84C=
ENST00000539099.2:c.1746-84C=	ENSP00000442630.1:n.1746-84C=
ENST00000541932.5:c.1661-84C=	ENSP00000437631.1:n.1661-84C=
ENST00000615840.4:c.1661-84C=	ENSP00000484039.1:n.1661-84C=
ENST00000615840.5:c.1661-84C=	ENSP00000484039.1:n.1661-84C=
ENST00000639477.1:c.1661-84C=	ENSP00000491097.1:n.1661-84C=
XM_011535014.1:c.1661-84C=	XP_011533316.1:n.1661-84C=
XM_017020485.1:c.1661-84C=	XP_016875974.1:n.1661-84C=