Canonical Allele Identifier: CA2120135626

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113915A= , CM000675.2:g.113113915A=	GRCh38
NC_000013.10:g.113768229A= , CM000675.1:g.113768229A=	GRCh37
NC_000013.9:g.112816230A=	NCBI36
NG_009262.1:g.13125A= , LRG_554:g.13125A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.319A= MANE Select	ENSP00000329546.4:p.Ile107=
ENST00000346342.7:c.319A=	ENSP00000329546.3:p.Ile107=
ENST00000375581.3:c.385A=	ENSP00000364731.3:p.Ile129=
ENST00000444337.1:c.*127A=	ENSP00000387669.1:n.*127A=
ENST00000473085.1:n.266A=
ENST00000479674.1:n.652A=
ENST00000541084.5:c.133A=	ENSP00000442051.2:p.Ile45=
NM_000131.4:c.385A= , LRG_554t1:c.385A=	NP_000122.1:p.Ile129=
NM_001267554.1:c.133A=	NP_001254483.1:p.Ile45=
NM_019616.3:c.319A= , LRG_554t2:c.319A=	NP_062562.1:p.Ile107=
NR_051961.1:n.406A=
XM_006719963.2:c.319A=	XP_006720026.1:p.Ile107=
XM_011537474.1:c.319A=	XP_011535776.1:p.Ile107=
XM_011537475.1:c.133A=	XP_011535777.1:p.Ile45=
XM_011537477.1:c.280A=	XP_011535779.1:p.Ile94=
XM_006719963.3:c.364A=	XP_006720026.2:p.Ile122=
XM_011537474.2:c.364A=	XP_011535776.2:p.Ile122=
XM_011537475.2:c.178A=	XP_011535777.2:p.Ile60=
NM_019616.4:c.319A= MANE Select	NP_062562.1:p.Ile107=
NR_051961.2:n.403A=
NM_001267554.2:c.133A=	NP_001254483.1:p.Ile45=