Canonical Allele Identifier: CA2120141997

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118518C= , CM000675.2:g.113118518C=	GRCh38
NC_000013.10:g.113772832C= , CM000675.1:g.113772832C=	GRCh37
NC_000013.9:g.112820833C=	NCBI36
NG_009258.1:g.720C= , LRG_548:g.720C=
NG_009262.1:g.17728C= , LRG_554:g.17728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.845C= MANE Select	ENSP00000329546.4:p.Ala282=
ENST00000346342.7:c.845C=	ENSP00000329546.3:p.Ala282=
ENST00000375581.3:c.911C=	ENSP00000364731.3:p.Ala304=
ENST00000541084.5:c.659C=	ENSP00000442051.2:p.Ala220=
NM_000131.4:c.911C= , LRG_554t1:c.911C=	NP_000122.1:p.Ala304=
NM_001267554.1:c.659C=	NP_001254483.1:p.Ala220=
NM_019616.3:c.845C= , LRG_554t2:c.845C=	NP_062562.1:p.Ala282=
NR_051961.1:n.932C=
XM_006719963.2:c.704C=	XP_006720026.1:p.Ala235=
XM_011537474.1:c.953C=	XP_011535776.1:p.Ala318=
XM_011537475.1:c.767C=	XP_011535777.1:p.Ala256=
XM_011537476.1:c.605C=	XP_011535778.1:p.Ala202=
XM_011537477.1:c.914C=	XP_011535779.1:p.Ala305=
XM_006719963.3:c.749C=	XP_006720026.2:p.Ala250=
XM_011537474.2:c.998C=	XP_011535776.2:p.Ala333=
XM_011537475.2:c.812C=	XP_011535777.2:p.Ala271=
XM_011537476.2:c.605C=	XP_011535778.1:p.Ala202=
NM_019616.4:c.845C= MANE Select	NP_062562.1:p.Ala282=
NR_051961.2:n.929C=
NM_001267554.2:c.659C=	NP_001254483.1:p.Ala220=