Canonical Allele Identifier: CA2120135678

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113941G= , CM000675.2:g.113113941G=	GRCh38
NC_000013.10:g.113768255G= , CM000675.1:g.113768255G=	GRCh37
NC_000013.9:g.112816256G=	NCBI36
NG_009262.1:g.13151G= , LRG_554:g.13151G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.345G= MANE Select	ENSP00000329546.4:p.Glu115=
ENST00000346342.7:c.345G=	ENSP00000329546.3:p.Glu115=
ENST00000375581.3:c.411G=	ENSP00000364731.3:p.Glu137=
ENST00000444337.1:c.*153G=	ENSP00000387669.1:n.*153G=
ENST00000473085.1:n.292G=
ENST00000479674.1:n.678G=
ENST00000541084.5:c.159G=	ENSP00000442051.2:p.Glu53=
NM_000131.4:c.411G= , LRG_554t1:c.411G=	NP_000122.1:p.Glu137=
NM_001267554.1:c.159G=	NP_001254483.1:p.Glu53=
NM_019616.3:c.345G= , LRG_554t2:c.345G=	NP_062562.1:p.Glu115=
NR_051961.1:n.432G=
XM_006719963.2:c.345G=	XP_006720026.1:p.Glu115=
XM_011537474.1:c.345G=	XP_011535776.1:p.Glu115=
XM_011537475.1:c.159G=	XP_011535777.1:p.Glu53=
XM_011537477.1:c.306G=	XP_011535779.1:p.Glu102=
XM_006719963.3:c.390G=	XP_006720026.2:p.Glu130=
XM_011537474.2:c.390G=	XP_011535776.2:p.Glu130=
XM_011537475.2:c.204G=	XP_011535777.2:p.Glu68=
NM_019616.4:c.345G= MANE Select	NP_062562.1:p.Glu115=
NR_051961.2:n.429G=
NM_001267554.2:c.159G=	NP_001254483.1:p.Glu53=