Canonical Allele Identifier: CA2120142285

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118655C= , CM000675.2:g.113118655C=	GRCh38
NC_000013.10:g.113772969C= , CM000675.1:g.113772969C=	GRCh37
NC_000013.9:g.112820970C=	NCBI36
NG_009258.1:g.857C= , LRG_548:g.857C=
NG_009262.1:g.17865C= , LRG_554:g.17865C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.982C= MANE Select	ENSP00000329546.4:p.Arg328=
ENST00000346342.7:c.982C=	ENSP00000329546.3:p.Arg328=
ENST00000375581.3:c.1048C=	ENSP00000364731.3:p.Arg350=
ENST00000541084.5:c.796C=	ENSP00000442051.2:p.Arg266=
NM_000131.4:c.1048C= , LRG_554t1:c.1048C=	NP_000122.1:p.Arg350=
NM_001267554.1:c.796C=	NP_001254483.1:p.Arg266=
NM_019616.3:c.982C= , LRG_554t2:c.982C=	NP_062562.1:p.Arg328=
NR_051961.1:n.1069C=
XM_006719963.2:c.841C=	XP_006720026.1:p.Arg281=
XM_011537474.1:c.1090C=	XP_011535776.1:p.Arg364=
XM_011537475.1:c.904C=	XP_011535777.1:p.Arg302=
XM_011537476.1:c.742C=	XP_011535778.1:p.Arg248=
XM_011537477.1:c.1051C=	XP_011535779.1:p.Arg351=
XM_006719963.3:c.886C=	XP_006720026.2:p.Arg296=
XM_011537474.2:c.1135C=	XP_011535776.2:p.Arg379=
XM_011537475.2:c.949C=	XP_011535777.2:p.Arg317=
XM_011537476.2:c.742C=	XP_011535778.1:p.Arg248=
NM_019616.4:c.982C= MANE Select	NP_062562.1:p.Arg328=
NR_051961.2:n.1066C=
NM_001267554.2:c.796C=	NP_001254483.1:p.Arg266=