Canonical Allele Identifier: CA612868293
Gene: F7 HGNC NCBI

Linked Data

dbSNP Id: rs1274330399

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118351_113118376del , CM000675.2:g.113118351_113118376del GRCh38
NC_000013.10:g.113772665_113772690del , CM000675.1:g.113772665_113772690del GRCh37
NC_000013.9:g.112820666_112820691del NCBI36
NG_009258.1:g.553_578del , LRG_548:g.553_578del
NG_009262.1:g.17561_17586del , LRG_554:g.17561_17586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.740-62_740-37del MANE Select ENSP00000329546.4:n.740-62_740-37del
ENST00000346342.7:c.740-62_740-37del ENSP00000329546.3:n.740-62_740-37del
ENST00000375581.3:c.806-62_806-37del ENSP00000364731.3:n.806-62_806-37del
ENST00000541084.5:c.554-62_554-37del ENSP00000442051.2:n.554-62_554-37del
NM_000131.4:c.806-62_806-37del , LRG_554t1:c.806-62_806-37del NP_000122.1:n.806-62_806-37del
NM_001267554.1:c.554-62_554-37del NP_001254483.1:n.554-62_554-37del
NM_019616.3:c.740-62_740-37del , LRG_554t2:c.740-62_740-37del NP_062562.1:n.740-62_740-37del
NR_051961.1:n.827-62_827-37del
XM_006719963.2:c.599-62_599-37del XP_006720026.1:n.599-62_599-37del
XM_011537474.1:c.848-62_848-37del XP_011535776.1:n.848-62_848-37del
XM_011537475.1:c.662-62_662-37del XP_011535777.1:n.662-62_662-37del
XM_011537476.1:c.500-62_500-37del XP_011535778.1:n.500-62_500-37del
XM_011537477.1:c.809-62_809-37del XP_011535779.1:n.809-62_809-37del
XM_006719963.3:c.644-62_644-37del XP_006720026.2:n.644-62_644-37del
XM_011537474.2:c.893-62_893-37del XP_011535776.2:n.893-62_893-37del
XM_011537475.2:c.707-62_707-37del XP_011535777.2:n.707-62_707-37del
XM_011537476.2:c.500-62_500-37del XP_011535778.1:n.500-62_500-37del
NM_019616.4:c.740-62_740-37del MANE Select NP_062562.1:n.740-62_740-37del
NR_051961.2:n.824-62_824-37del
NM_001267554.2:c.554-62_554-37del NP_001254483.1:n.554-62_554-37del