Canonical Allele Identifier: CA2120142011

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118527G= , CM000675.2:g.113118527G=	GRCh38
NC_000013.10:g.113772841G= , CM000675.1:g.113772841G=	GRCh37
NC_000013.9:g.112820842G=	NCBI36
NG_009258.1:g.729G= , LRG_548:g.729G=
NG_009262.1:g.17737G= , LRG_554:g.17737G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.854G= MANE Select	ENSP00000329546.4:p.Arg285=
ENST00000346342.7:c.854G=	ENSP00000329546.3:p.Arg285=
ENST00000375581.3:c.920G=	ENSP00000364731.3:p.Arg307=
ENST00000541084.5:c.668G=	ENSP00000442051.2:p.Arg223=
NM_000131.4:c.920G= , LRG_554t1:c.920G=	NP_000122.1:p.Arg307=
NM_001267554.1:c.668G=	NP_001254483.1:p.Arg223=
NM_019616.3:c.854G= , LRG_554t2:c.854G=	NP_062562.1:p.Arg285=
NR_051961.1:n.941G=
XM_006719963.2:c.713G=	XP_006720026.1:p.Arg238=
XM_011537474.1:c.962G=	XP_011535776.1:p.Arg321=
XM_011537475.1:c.776G=	XP_011535777.1:p.Arg259=
XM_011537476.1:c.614G=	XP_011535778.1:p.Arg205=
XM_011537477.1:c.923G=	XP_011535779.1:p.Arg308=
XM_006719963.3:c.758G=	XP_006720026.2:p.Arg253=
XM_011537474.2:c.1007G=	XP_011535776.2:p.Arg336=
XM_011537475.2:c.821G=	XP_011535777.2:p.Arg274=
XM_011537476.2:c.614G=	XP_011535778.1:p.Arg205=
NM_019616.4:c.854G= MANE Select	NP_062562.1:p.Arg285=
NR_051961.2:n.938G=
NM_001267554.2:c.668G=	NP_001254483.1:p.Arg223=