Canonical Allele Identifier: CA2623808560
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118303del , CM000675.2:g.113118303del GRCh38
NC_000013.10:g.113772617del , CM000675.1:g.113772617del GRCh37
NC_000013.9:g.112820618del NCBI36
NG_009258.1:g.505del , LRG_548:g.505del
NG_009262.1:g.17513del , LRG_554:g.17513del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.740-110del MANE Select ENSP00000329546.4:n.740-110del
ENST00000346342.7:c.740-110del ENSP00000329546.3:n.740-110del
ENST00000375581.3:c.806-110del ENSP00000364731.3:n.806-110del
ENST00000541084.5:c.554-110del ENSP00000442051.2:n.554-110del
NM_000131.4:c.806-110del , LRG_554t1:c.806-110del NP_000122.1:n.806-110del
NM_001267554.1:c.554-110del NP_001254483.1:n.554-110del
NM_019616.3:c.740-110del , LRG_554t2:c.740-110del NP_062562.1:n.740-110del
NR_051961.1:n.827-110del
XM_006719963.2:c.599-110del XP_006720026.1:n.599-110del
XM_011537474.1:c.848-110del XP_011535776.1:n.848-110del
XM_011537475.1:c.662-110del XP_011535777.1:n.662-110del
XM_011537476.1:c.500-110del XP_011535778.1:n.500-110del
XM_011537477.1:c.809-110del XP_011535779.1:n.809-110del
XM_006719963.3:c.644-110del XP_006720026.2:n.644-110del
XM_011537474.2:c.893-110del XP_011535776.2:n.893-110del
XM_011537475.2:c.707-110del XP_011535777.2:n.707-110del
XM_011537476.2:c.500-110del XP_011535778.1:n.500-110del
NM_019616.4:c.740-110del MANE Select NP_062562.1:n.740-110del
NR_051961.2:n.824-110del
NM_001267554.2:c.554-110del NP_001254483.1:n.554-110del