Canonical Allele Identifier: CA2120135665

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113933G= , CM000675.2:g.113113933G=	GRCh38
NC_000013.10:g.113768247G= , CM000675.1:g.113768247G=	GRCh37
NC_000013.9:g.112816248G=	NCBI36
NG_009262.1:g.13143G= , LRG_554:g.13143G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.337G= MANE Select	ENSP00000329546.4:p.Ala113=
ENST00000346342.7:c.337G=	ENSP00000329546.3:p.Ala113=
ENST00000375581.3:c.403G=	ENSP00000364731.3:p.Ala135=
ENST00000444337.1:c.*145G=	ENSP00000387669.1:n.*145G=
ENST00000473085.1:n.284G=
ENST00000479674.1:n.670G=
ENST00000541084.5:c.151G=	ENSP00000442051.2:p.Ala51=
NM_000131.4:c.403G= , LRG_554t1:c.403G=	NP_000122.1:p.Ala135=
NM_001267554.1:c.151G=	NP_001254483.1:p.Ala51=
NM_019616.3:c.337G= , LRG_554t2:c.337G=	NP_062562.1:p.Ala113=
NR_051961.1:n.424G=
XM_006719963.2:c.337G=	XP_006720026.1:p.Ala113=
XM_011537474.1:c.337G=	XP_011535776.1:p.Ala113=
XM_011537475.1:c.151G=	XP_011535777.1:p.Ala51=
XM_011537477.1:c.298G=	XP_011535779.1:p.Ala100=
XM_006719963.3:c.382G=	XP_006720026.2:p.Ala128=
XM_011537474.2:c.382G=	XP_011535776.2:p.Ala128=
XM_011537475.2:c.196G=	XP_011535777.2:p.Ala66=
NM_019616.4:c.337G= MANE Select	NP_062562.1:p.Ala113=
NR_051961.2:n.421G=
NM_001267554.2:c.151G=	NP_001254483.1:p.Ala51=