Canonical Allele Identifier: CA2623810108
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119282_113119287del , CM000675.2:g.113119282_113119287del GRCh38
NC_000013.10:g.113773596_113773601del , CM000675.1:g.113773596_113773601del GRCh37
NC_000013.9:g.112821597_112821602del NCBI36
NG_009258.1:g.1484_1489del , LRG_548:g.1484_1489del
NG_009262.1:g.18492_18497del , LRG_554:g.18492_18497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*274_*279del MANE Select ENSP00000329546.4:n.*274_*279del
ENST00000346342.7:c.*274_*279del ENSP00000329546.3:n.*274_*279del
ENST00000375581.3:c.*274_*279del ENSP00000364731.3:n.*274_*279del
ENST00000541084.5:c.*274_*279del ENSP00000442051.2:n.*274_*279del
NM_000131.4:c.*274_*279del , LRG_554t1:c.*274_*279del NP_000122.1:n.*274_*279del
NM_001267554.1:c.*274_*279del NP_001254483.1:n.*274_*279del
NM_019616.3:c.*274_*279del , LRG_554t2:c.*274_*279del NP_062562.1:n.*274_*279del
NR_051961.1:n.1696_1701del
XM_006719963.2:c.*274_*279del XP_006720026.1:n.*274_*279del
XM_011537474.1:c.*274_*279del XP_011535776.1:n.*274_*279del
XM_011537475.1:c.*274_*279del XP_011535777.1:n.*274_*279del
XM_011537476.1:c.*274_*279del XP_011535778.1:n.*274_*279del
XM_011537477.1:c.*274_*279del XP_011535779.1:n.*274_*279del
XM_006719963.3:c.*274_*279del XP_006720026.2:n.*274_*279del
XM_011537474.2:c.*274_*279del XP_011535776.2:n.*274_*279del
XM_011537475.2:c.*274_*279del XP_011535777.2:n.*274_*279del
XM_011537476.2:c.*274_*279del XP_011535778.1:n.*274_*279del
NM_019616.4:c.*274_*279del MANE Select NP_062562.1:n.*274_*279del
NR_051961.2:n.1693_1698del
NM_001267554.2:c.*274_*279del NP_001254483.1:n.*274_*279del