Canonical Allele Identifier: CA2623803363

Gene: F7

Linked Data

• gnomAD v4: 13-113113796-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113796C>A , CM000675.2:g.113113796C>A	GRCh38
NC_000013.10:g.113768110C>A , CM000675.1:g.113768110C>A	GRCh37
NC_000013.9:g.112816111C>A	NCBI36
NG_009262.1:g.13006C>A , LRG_554:g.13006C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.250+20C>A MANE Select	ENSP00000329546.4:n.250+20C>A
ENST00000346342.7:c.250+20C>A	ENSP00000329546.3:n.250+20C>A
ENST00000375581.3:c.316+20C>A	ENSP00000364731.3:n.316+20C>A
ENST00000444337.1:c.*8C>A	ENSP00000387669.1:n.*8C>A
ENST00000473085.1:n.197+20C>A
ENST00000479674.1:n.533C>A
ENST00000541084.5:c.65-51C>A	ENSP00000442051.2:n.65-51C>A
NM_000131.4:c.316+20C>A , LRG_554t1:c.316+20C>A	NP_000122.1:n.316+20C>A
NM_001267554.1:c.65-51C>A	NP_001254483.1:n.65-51C>A
NM_019616.3:c.250+20C>A , LRG_554t2:c.250+20C>A	NP_062562.1:n.250+20C>A
NR_051961.1:n.287C>A
XM_006719963.2:c.250+20C>A	XP_006720026.1:n.250+20C>A
XM_011537474.1:c.250+20C>A	XP_011535776.1:n.250+20C>A
XM_011537475.1:c.65-51C>A	XP_011535777.1:n.65-51C>A
XM_011537477.1:c.212-51C>A	XP_011535779.1:n.212-51C>A
XM_006719963.3:c.295+20C>A	XP_006720026.2:n.295+20C>A
XM_011537474.2:c.295+20C>A	XP_011535776.2:n.295+20C>A
XM_011537475.2:c.110-51C>A	XP_011535777.2:n.110-51C>A
NM_019616.4:c.250+20C>A MANE Select	NP_062562.1:n.250+20C>A
NR_051961.2:n.284C>A
NM_001267554.2:c.65-51C>A	NP_001254483.1:n.65-51C>A