Canonical Allele Identifier: CA2623809663

Gene: F7

Linked Data

• gnomAD v4: 13-113119115-AGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119116_113119118del , CM000675.2:g.113119116_113119118del	GRCh38
NC_000013.10:g.113773430_113773432del , CM000675.1:g.113773430_113773432del	GRCh37
NC_000013.9:g.112821431_112821433del	NCBI36
NG_009258.1:g.1318_1320del , LRG_548:g.1318_1320del
NG_009262.1:g.18326_18328del , LRG_554:g.18326_18328del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*108_*110del MANE Select	ENSP00000329546.4:n.*108_*110del
ENST00000346342.7:c.*108_*110del	ENSP00000329546.3:n.*108_*110del
ENST00000375581.3:c.*108_*110del	ENSP00000364731.3:n.*108_*110del
ENST00000541084.5:c.*108_*110del	ENSP00000442051.2:n.*108_*110del
NM_000131.4:c.*108_*110del , LRG_554t1:c.*108_*110del	NP_000122.1:n.*108_*110del
NM_001267554.1:c.*108_*110del	NP_001254483.1:n.*108_*110del
NM_019616.3:c.*108_*110del , LRG_554t2:c.*108_*110del	NP_062562.1:n.*108_*110del
NR_051961.1:n.1530_1532del
XM_006719963.2:c.*108_*110del	XP_006720026.1:n.*108_*110del
XM_011537474.1:c.*108_*110del	XP_011535776.1:n.*108_*110del
XM_011537475.1:c.*108_*110del	XP_011535777.1:n.*108_*110del
XM_011537476.1:c.*108_*110del	XP_011535778.1:n.*108_*110del
XM_011537477.1:c.*108_*110del	XP_011535779.1:n.*108_*110del
XM_006719963.3:c.*108_*110del	XP_006720026.2:n.*108_*110del
XM_011537474.2:c.*108_*110del	XP_011535776.2:n.*108_*110del
XM_011537475.2:c.*108_*110del	XP_011535777.2:n.*108_*110del
XM_011537476.2:c.*108_*110del	XP_011535778.1:n.*108_*110del
NM_019616.4:c.*108_*110del MANE Select	NP_062562.1:n.*108_*110del
NR_051961.2:n.1527_1529del
NM_001267554.2:c.*108_*110del	NP_001254483.1:n.*108_*110del