Canonical Allele Identifier: CA960419801
Gene: F10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149375_113149376del , CM000675.2:g.113149375_113149376del GRCh38
NC_000013.10:g.113803689_113803690del , CM000675.1:g.113803689_113803690del GRCh37
NC_000013.9:g.112851690_112851691del NCBI36
NG_009258.1:g.31577_31578del , LRG_548:g.31577_31578del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1325_1326del MANE Select ENSP00000364709.3:p.Gly442ValfsTer4
ENST00000375551.7:c.*316_*317del ENSP00000364701.3:n.*316_*317del
ENST00000375559.7:c.1325_1326del ENSP00000364709.3:p.Gly442ValfsTer4
ENST00000409306.5:c.*316_*317del ENSP00000387092.1:n.*316_*317del
NM_000504.3:c.1325_1326del , LRG_548t1:c.1325_1326del NP_000495.1:p.Gly442ValfsTer4
NM_001312674.1:c.1193_1194del NP_001299603.1:p.Gly398ValfsTer4
NM_001312675.1:c.*316_*317del NP_001299604.1:n.*316_*317del
NM_000504.4:c.1325_1326del MANE Select NP_000495.1:p.Gly442ValfsTer4
NM_001312674.2:c.1193_1194del NP_001299603.1:p.Gly398ValfsTer4
NM_001312675.2:c.*316_*317del NP_001299604.1:n.*316_*317del