Canonical Allele Identifier: CA10642916
Gene: F7 HGNC NCBI

Linked Data

ClinVar Variation Id: 311252
ClinVar RCV Id: RCV000314976
dbSNP Id: rs886049998

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119859_113119863del , CM000675.2:g.113119859_113119863del GRCh38
NC_000013.10:g.113774173_113774177del , CM000675.1:g.113774173_113774177del GRCh37
NC_000013.9:g.112822174_112822178del NCBI36
NG_009258.1:g.2061_2065del , LRG_548:g.2061_2065del
NG_009262.1:g.19069_19073del , LRG_554:g.19069_19073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*851_*855del MANE Select ENSP00000329546.4:n.*851_*855del
ENST00000346342.7:c.*851_*855del ENSP00000329546.3:n.*851_*855del
ENST00000375581.3:c.*851_*855del ENSP00000364731.3:n.*851_*855del
ENST00000541084.5:c.*851_*855del ENSP00000442051.2:n.*851_*855del
NM_000131.4:c.*851_*855del , LRG_554t1:c.*851_*855del NP_000122.1:n.*851_*855del
NM_001267554.1:c.*851_*855del NP_001254483.1:n.*851_*855del
NM_019616.3:c.*851_*855del , LRG_554t2:c.*851_*855del NP_062562.1:n.*851_*855del
NR_051961.1:n.2273_2277del
XM_006719963.2:c.*851_*855del XP_006720026.1:n.*851_*855del
XM_011537474.1:c.*851_*855del XP_011535776.1:n.*851_*855del
XM_011537475.1:c.*851_*855del XP_011535777.1:n.*851_*855del
XM_011537476.1:c.*851_*855del XP_011535778.1:n.*851_*855del
XM_011537477.1:c.*851_*855del XP_011535779.1:n.*851_*855del
XM_006719963.3:c.*851_*855del XP_006720026.2:n.*851_*855del
XM_011537474.2:c.*851_*855del XP_011535776.2:n.*851_*855del
XM_011537475.2:c.*851_*855del XP_011535777.2:n.*851_*855del
XM_011537476.2:c.*851_*855del XP_011535778.1:n.*851_*855del
NM_019616.4:c.*851_*855del MANE Select NP_062562.1:n.*851_*855del
NR_051961.2:n.2270_2274del
NM_001267554.2:c.*851_*855del NP_001254483.1:n.*851_*855del