Canonical Allele Identifier: CA2120135431

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113783G= , CM000675.2:g.113113783G=	GRCh38
NC_000013.10:g.113768097G= , CM000675.1:g.113768097G=	GRCh37
NC_000013.9:g.112816098G=	NCBI36
NG_009262.1:g.12993G= , LRG_554:g.12993G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.250+7G= MANE Select	ENSP00000329546.4:n.250+7G=
ENST00000346342.7:c.250+7G=	ENSP00000329546.3:n.250+7G=
ENST00000375581.3:c.316+7G=	ENSP00000364731.3:n.316+7G=
ENST00000444337.1:c.220G=	ENSP00000387669.1:p.Gly74=
ENST00000473085.1:n.197+7G=
ENST00000479674.1:n.520G=
ENST00000541084.5:c.65-64G=	ENSP00000442051.2:n.65-64G=
NM_000131.4:c.316+7G= , LRG_554t1:c.316+7G=	NP_000122.1:n.316+7G=
NM_001267554.1:c.65-64G=	NP_001254483.1:n.65-64G=
NM_019616.3:c.250+7G= , LRG_554t2:c.250+7G=	NP_062562.1:n.250+7G=
NR_051961.1:n.274G=
XM_006719963.2:c.250+7G=	XP_006720026.1:n.250+7G=
XM_011537474.1:c.250+7G=	XP_011535776.1:n.250+7G=
XM_011537475.1:c.65-64G=	XP_011535777.1:n.65-64G=
XM_011537477.1:c.212-64G=	XP_011535779.1:n.212-64G=
XM_006719963.3:c.295+7G=	XP_006720026.2:n.295+7G=
XM_011537474.2:c.295+7G=	XP_011535776.2:n.295+7G=
XM_011537475.2:c.110-64G=	XP_011535777.2:n.110-64G=
NM_019616.4:c.250+7G= MANE Select	NP_062562.1:n.250+7G=
NR_051961.2:n.271G=
NM_001267554.2:c.65-64G=	NP_001254483.1:n.65-64G=