Canonical Allele Identifier: CA2120141743

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118441G= , CM000675.2:g.113118441G=	GRCh38
NC_000013.10:g.113772755G= , CM000675.1:g.113772755G=	GRCh37
NC_000013.9:g.112820756G=	NCBI36
NG_009258.1:g.643G= , LRG_548:g.643G=
NG_009262.1:g.17651G= , LRG_554:g.17651G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.768G= MANE Select	ENSP00000329546.4:p.Gly256=
ENST00000346342.7:c.768G=	ENSP00000329546.3:p.Gly256=
ENST00000375581.3:c.834G=	ENSP00000364731.3:p.Gly278=
ENST00000541084.5:c.582G=	ENSP00000442051.2:p.Gly194=
NM_000131.4:c.834G= , LRG_554t1:c.834G=	NP_000122.1:p.Gly278=
NM_001267554.1:c.582G=	NP_001254483.1:p.Gly194=
NM_019616.3:c.768G= , LRG_554t2:c.768G=	NP_062562.1:p.Gly256=
NR_051961.1:n.855G=
XM_006719963.2:c.627G=	XP_006720026.1:p.Gly209=
XM_011537474.1:c.876G=	XP_011535776.1:p.Gly292=
XM_011537475.1:c.690G=	XP_011535777.1:p.Gly230=
XM_011537476.1:c.528G=	XP_011535778.1:p.Gly176=
XM_011537477.1:c.837G=	XP_011535779.1:p.Gly279=
XM_006719963.3:c.672G=	XP_006720026.2:p.Gly224=
XM_011537474.2:c.921G=	XP_011535776.2:p.Gly307=
XM_011537475.2:c.735G=	XP_011535777.2:p.Gly245=
XM_011537476.2:c.528G=	XP_011535778.1:p.Gly176=
NM_019616.4:c.768G= MANE Select	NP_062562.1:p.Gly256=
NR_051961.2:n.852G=
NM_001267554.2:c.582G=	NP_001254483.1:p.Gly194=