Canonical Allele Identifier: CA2120140247

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149155G= , CM000675.2:g.113149155G=	GRCh38
NC_000013.10:g.113803469G= , CM000675.1:g.113803469G=	GRCh37
NC_000013.9:g.112851470G=	NCBI36
NG_009258.1:g.31357G= , LRG_548:g.31357G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1105G= MANE Select	ENSP00000364709.3:p.Glu369=
ENST00000375551.7:c.*96G=	ENSP00000364701.3:n.*96G=
ENST00000375559.7:c.1105G=	ENSP00000364709.3:p.Glu369=
ENST00000409306.5:c.*96G=	ENSP00000387092.1:n.*96G=
NM_000504.3:c.1105G= , LRG_548t1:c.1105G=	NP_000495.1:p.Glu369=
NM_001312674.1:c.973G=	NP_001299603.1:p.Glu325=
NM_001312675.1:c.*96G=	NP_001299604.1:n.*96G=
NM_000504.4:c.1105G= MANE Select	NP_000495.1:p.Glu369=
NM_001312674.2:c.973G=	NP_001299603.1:p.Glu325=
NM_001312675.2:c.*96G=	NP_001299604.1:n.*96G=