Canonical Allele Identifier: CA2081036644

Gene: FLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28483931A= , CM000675.2:g.28483931A=	GRCh38
NC_000013.10:g.29058068A= , CM000675.1:g.29058068A=	GRCh37
NC_000013.9:g.27956068A=	NCBI36
NG_012003.1:g.16198T=

Transcript Alleles

HGVS	Amino-acid Change
NM_002019.4:c.64+10849T= MANE Select	NP_002010.2:n.64+10849T=
ENST00000282397.9:c.64+10849T= MANE Select	ENSP00000282397.4:n.64+10849T=
NM_001159920.1:c.64+10849T=	NP_001153392.1:n.64+10849T=
NM_001159920.2:c.64+10849T=	NP_001153392.1:n.64+10849T=
NM_001160030.1:c.64+10849T=	NP_001153502.1:n.64+10849T=
NM_001160030.2:c.64+10849T=	NP_001153502.1:n.64+10849T=
NM_001160031.1:c.64+10849T=	NP_001153503.1:n.64+10849T=
ENST00000282397.8:c.64+10849T=	ENSP00000282397.4:n.64+10849T=
ENST00000539099.1:c.64+10849T=	ENSP00000442630.1:n.64+10849T=
ENST00000539099.2:c.64+10849T=	ENSP00000442630.1:n.64+10849T=
ENST00000541932.5:c.64+10849T=	ENSP00000437631.1:n.64+10849T=
ENST00000615840.4:c.64+10849T=	ENSP00000484039.1:n.64+10849T=
ENST00000615840.5:c.64+10849T=	ENSP00000484039.1:n.64+10849T=
ENST00000639477.1:c.64+10849T=	ENSP00000491097.1:n.64+10849T=
XM_011535014.1:c.64+10849T=	XP_011533316.1:n.64+10849T=
XM_017020485.1:c.64+10849T=	XP_016875974.1:n.64+10849T=