Canonical Allele Identifier: CA2120144373

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119664C= , CM000675.2:g.113119664C=	GRCh38
NC_000013.10:g.113773978C= , CM000675.1:g.113773978C=	GRCh37
NC_000013.9:g.112821979C=	NCBI36
NG_009258.1:g.1866C= , LRG_548:g.1866C=
NG_009262.1:g.18874C= , LRG_554:g.18874C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*656C= MANE Select	ENSP00000329546.4:n.*656C=
ENST00000346342.7:c.*656C=	ENSP00000329546.3:n.*656C=
ENST00000375581.3:c.*656C=	ENSP00000364731.3:n.*656C=
ENST00000541084.5:c.*656C=	ENSP00000442051.2:n.*656C=
NM_000131.4:c.*656C= , LRG_554t1:c.*656C=	NP_000122.1:n.*656C=
NM_001267554.1:c.*656C=	NP_001254483.1:n.*656C=
NM_019616.3:c.*656C= , LRG_554t2:c.*656C=	NP_062562.1:n.*656C=
NR_051961.1:n.2078C=
XM_006719963.2:c.*656C=	XP_006720026.1:n.*656C=
XM_011537474.1:c.*656C=	XP_011535776.1:n.*656C=
XM_011537475.1:c.*656C=	XP_011535777.1:n.*656C=
XM_011537476.1:c.*656C=	XP_011535778.1:n.*656C=
XM_011537477.1:c.*656C=	XP_011535779.1:n.*656C=
XM_006719963.3:c.*656C=	XP_006720026.2:n.*656C=
XM_011537474.2:c.*656C=	XP_011535776.2:n.*656C=
XM_011537475.2:c.*656C=	XP_011535777.2:n.*656C=
XM_011537476.2:c.*656C=	XP_011535778.1:n.*656C=
NM_019616.4:c.*656C= MANE Select	NP_062562.1:n.*656C=
NR_051961.2:n.2075C=
NM_001267554.2:c.*656C=	NP_001254483.1:n.*656C=