Canonical Allele Identifier: CA2623810410
Gene: F10 HGNC NCBI

Linked Data

gnomAD v4: 13-113149452-ACCAGGGGCTTGCCCAAGGCCAAGAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149456_113149480del , CM000675.2:g.113149456_113149480del GRCh38
NC_000013.10:g.113803770_113803794del , CM000675.1:g.113803770_113803794del GRCh37
NC_000013.9:g.112851771_112851795del NCBI36
NG_009258.1:g.31658_31682del , LRG_548:g.31658_31682del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1406_1430del MANE Select ENSP00000364709.3:p.Arg469MetfsTer6
ENST00000375551.7:c.*397_*421del ENSP00000364701.3:n.*397_*421del
ENST00000375559.7:c.1406_1430del ENSP00000364709.3:p.Arg469MetfsTer6
NM_000504.3:c.1406_1430del , LRG_548t1:c.1406_1430del NP_000495.1:p.Arg469MetfsTer6
NM_001312674.1:c.1274_1298del NP_001299603.1:p.Arg425MetfsTer6
NM_001312675.1:c.*397_*421del NP_001299604.1:n.*397_*421del
NM_000504.4:c.1406_1430del MANE Select NP_000495.1:p.Arg469MetfsTer6
NM_001312674.2:c.1274_1298del NP_001299603.1:p.Arg425MetfsTer6
NM_001312675.2:c.*397_*421del NP_001299604.1:n.*397_*421del
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