Canonical Allele Identifier: CA2120141884

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118468G= , CM000675.2:g.113118468G=	GRCh38
NC_000013.10:g.113772782G= , CM000675.1:g.113772782G=	GRCh37
NC_000013.9:g.112820783G=	NCBI36
NG_009258.1:g.670G= , LRG_548:g.670G=
NG_009262.1:g.17678G= , LRG_554:g.17678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.795G= MANE Select	ENSP00000329546.4:p.Gln265=
ENST00000346342.7:c.795G=	ENSP00000329546.3:p.Gln265=
ENST00000375581.3:c.861G=	ENSP00000364731.3:p.Gln287=
ENST00000541084.5:c.609G=	ENSP00000442051.2:p.Gln203=
NM_000131.4:c.861G= , LRG_554t1:c.861G=	NP_000122.1:p.Gln287=
NM_001267554.1:c.609G=	NP_001254483.1:p.Gln203=
NM_019616.3:c.795G= , LRG_554t2:c.795G=	NP_062562.1:p.Gln265=
NR_051961.1:n.882G=
XM_006719963.2:c.654G=	XP_006720026.1:p.Gln218=
XM_011537474.1:c.903G=	XP_011535776.1:p.Gln301=
XM_011537475.1:c.717G=	XP_011535777.1:p.Gln239=
XM_011537476.1:c.555G=	XP_011535778.1:p.Gln185=
XM_011537477.1:c.864G=	XP_011535779.1:p.Gln288=
XM_006719963.3:c.699G=	XP_006720026.2:p.Gln233=
XM_011537474.2:c.948G=	XP_011535776.2:p.Gln316=
XM_011537475.2:c.762G=	XP_011535777.2:p.Gln254=
XM_011537476.2:c.555G=	XP_011535778.1:p.Gln185=
NM_019616.4:c.795G= MANE Select	NP_062562.1:p.Gln265=
NR_051961.2:n.879G=
NM_001267554.2:c.609G=	NP_001254483.1:p.Gln203=