Canonical Allele Identifier: CA655989225

Gene: F7

Linked Data

• COSMIC: COSN8587180

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113117417C>A , CM000675.2:g.113117417C>A	GRCh38
NC_000013.10:g.113771731C>A , CM000675.1:g.113771731C>A	GRCh37
NC_000013.9:g.112819732C>A	NCBI36
NG_009262.1:g.16627C>A , LRG_554:g.16627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.616-56C>A MANE Select	ENSP00000329546.4:n.616-56C>A
ENST00000346342.7:c.616-56C>A	ENSP00000329546.3:n.616-56C>A
ENST00000375581.3:c.682-56C>A	ENSP00000364731.3:n.682-56C>A
ENST00000541084.5:c.430-56C>A	ENSP00000442051.2:n.430-56C>A
NM_000131.4:c.682-56C>A , LRG_554t1:c.682-56C>A	NP_000122.1:n.682-56C>A
NM_001267554.1:c.430-56C>A	NP_001254483.1:n.430-56C>A
NM_019616.3:c.616-56C>A , LRG_554t2:c.616-56C>A	NP_062562.1:n.616-56C>A
NR_051961.1:n.703-56C>A
XM_006719963.2:c.475-56C>A	XP_006720026.1:n.475-56C>A
XM_011537474.1:c.724-56C>A	XP_011535776.1:n.724-56C>A
XM_011537475.1:c.538-56C>A	XP_011535777.1:n.538-56C>A
XM_011537476.1:c.376-56C>A	XP_011535778.1:n.376-56C>A
XM_011537477.1:c.685-56C>A	XP_011535779.1:n.685-56C>A
XM_006719963.3:c.520-56C>A	XP_006720026.2:n.520-56C>A
XM_011537474.2:c.769-56C>A	XP_011535776.2:n.769-56C>A
XM_011537475.2:c.583-56C>A	XP_011535777.2:n.583-56C>A
XM_011537476.2:c.376-56C>A	XP_011535778.1:n.376-56C>A
NM_019616.4:c.616-56C>A MANE Select	NP_062562.1:n.616-56C>A
NR_051961.2:n.700-56C>A
NM_001267554.2:c.430-56C>A	NP_001254483.1:n.430-56C>A