Canonical Allele Identifier: CA2120140050

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113117413G= , CM000675.2:g.113117413G=	GRCh38
NC_000013.10:g.113771727G= , CM000675.1:g.113771727G=	GRCh37
NC_000013.9:g.112819728G=	NCBI36
NG_009262.1:g.16623G= , LRG_554:g.16623G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.616-60G= MANE Select	ENSP00000329546.4:n.616-60G=
ENST00000346342.7:c.616-60G=	ENSP00000329546.3:n.616-60G=
ENST00000375581.3:c.682-60G=	ENSP00000364731.3:n.682-60G=
ENST00000541084.5:c.430-60G=	ENSP00000442051.2:n.430-60G=
NM_000131.4:c.682-60G= , LRG_554t1:c.682-60G=	NP_000122.1:n.682-60G=
NM_001267554.1:c.430-60G=	NP_001254483.1:n.430-60G=
NM_019616.3:c.616-60G= , LRG_554t2:c.616-60G=	NP_062562.1:n.616-60G=
NR_051961.1:n.703-60G=
XM_006719963.2:c.475-60G=	XP_006720026.1:n.475-60G=
XM_011537474.1:c.724-60G=	XP_011535776.1:n.724-60G=
XM_011537475.1:c.538-60G=	XP_011535777.1:n.538-60G=
XM_011537476.1:c.376-60G=	XP_011535778.1:n.376-60G=
XM_011537477.1:c.685-60G=	XP_011535779.1:n.685-60G=
XM_006719963.3:c.520-60G=	XP_006720026.2:n.520-60G=
XM_011537474.2:c.769-60G=	XP_011535776.2:n.769-60G=
XM_011537475.2:c.583-60G=	XP_011535777.2:n.583-60G=
XM_011537476.2:c.376-60G=	XP_011535778.1:n.376-60G=
NM_019616.4:c.616-60G= MANE Select	NP_062562.1:n.616-60G=
NR_051961.2:n.700-60G=
NM_001267554.2:c.430-60G=	NP_001254483.1:n.430-60G=