Canonical Allele Identifier: CA2120141691

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118430G= , CM000675.2:g.113118430G=	GRCh38
NC_000013.10:g.113772744G= , CM000675.1:g.113772744G=	GRCh37
NC_000013.9:g.112820745G=	NCBI36
NG_009258.1:g.632G= , LRG_548:g.632G=
NG_009262.1:g.17640G= , LRG_554:g.17640G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.757G= MANE Select	ENSP00000329546.4:p.Glu253=
ENST00000346342.7:c.757G=	ENSP00000329546.3:p.Glu253=
ENST00000375581.3:c.823G=	ENSP00000364731.3:p.Glu275=
ENST00000541084.5:c.571G=	ENSP00000442051.2:p.Glu191=
NM_000131.4:c.823G= , LRG_554t1:c.823G=	NP_000122.1:p.Glu275=
NM_001267554.1:c.571G=	NP_001254483.1:p.Glu191=
NM_019616.3:c.757G= , LRG_554t2:c.757G=	NP_062562.1:p.Glu253=
NR_051961.1:n.844G=
XM_006719963.2:c.616G=	XP_006720026.1:p.Glu206=
XM_011537474.1:c.865G=	XP_011535776.1:p.Glu289=
XM_011537475.1:c.679G=	XP_011535777.1:p.Glu227=
XM_011537476.1:c.517G=	XP_011535778.1:p.Glu173=
XM_011537477.1:c.826G=	XP_011535779.1:p.Glu276=
XM_006719963.3:c.661G=	XP_006720026.2:p.Glu221=
XM_011537474.2:c.910G=	XP_011535776.2:p.Glu304=
XM_011537475.2:c.724G=	XP_011535777.2:p.Glu242=
XM_011537476.2:c.517G=	XP_011535778.1:p.Glu173=
NM_019616.4:c.757G= MANE Select	NP_062562.1:p.Glu253=
NR_051961.2:n.841G=
NM_001267554.2:c.571G=	NP_001254483.1:p.Glu191=