Canonical Allele Identifier: CA2614112102
Gene: FERMT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64223152del , CM000673.2:g.64223152del GRCh38
NC_000011.9:g.63990624del , CM000673.1:g.63990624del GRCh37
NC_000011.8:g.63747200del NCBI36
NG_016360.1:g.21473del , LRG_180:g.21473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279227.10:c.1787del ENSP00000279227.5:p.Asn596ThrfsTer?
ENST00000540554.2:n.3299del
ENST00000541252.2:c.1235del ENSP00000438885.2:p.Asn412ThrfsTer?
ENST00000544997.6:c.1775del ENSP00000445778.2:p.Asn592ThrfsTer?
ENST00000545896.2:c.339del ENSP00000440209.2:p.Gln113HisfsTer?
ENST00000546255.2:n.2079del
ENST00000698845.1:c.*970del ENSP00000513981.1:n.*970del
ENST00000698846.1:n.2021del
ENST00000698847.1:c.*1180del ENSP00000513982.1:n.*1180del
ENST00000698850.1:n.3796del
ENST00000698852.1:c.1775del ENSP00000513984.1:p.Asn592ThrfsTer?
ENST00000698853.1:c.*1004del ENSP00000513985.1:n.*1004del
ENST00000698854.1:c.*1105del ENSP00000513986.1:n.*1105del
ENST00000698855.1:n.3427del
ENST00000698856.1:n.3121del
ENST00000698859.1:n.2285del
ENST00000698860.1:c.1787del ENSP00000513988.1:p.Asn596ThrfsTer?
ENST00000698861.1:c.1775del ENSP00000513989.1:p.Asn592ThrfsTer?
ENST00000698862.1:c.*1071del ENSP00000513990.1:n.*1071del
ENST00000698863.1:c.1775del ENSP00000513991.1:p.Asn592ThrfsTer?
ENST00000698864.1:n.2336del
ENST00000698865.1:c.1796del ENSP00000513992.1:p.Asn599ThrfsTer?
ENST00000698866.1:c.*1563del ENSP00000513993.1:n.*1563del
ENST00000698867.1:n.5750del
ENST00000698868.1:c.1640del ENSP00000513994.1:p.Asn547ThrfsTer?
ENST00000698869.1:c.1541del ENSP00000513995.1:p.Asn514ThrfsTer?
ENST00000698870.1:c.1775del ENSP00000513996.1:p.Asn592ThrfsTer?
ENST00000698871.1:n.2298del
ENST00000698872.1:c.*564del ENSP00000513997.1:n.*564del
ENST00000698873.1:c.*970del ENSP00000513998.1:n.*970del
ENST00000698874.1:c.1235del ENSP00000513999.1:p.Asn412ThrfsTer?
ENST00000698875.1:n.1635del
ENST00000698876.1:n.1823del
ENST00000698877.1:n.1343del
ENST00000698878.1:c.1769del ENSP00000514000.1:p.Asn590ThrfsTer?
ENST00000698880.1:c.1643del
ENST00000345728.10:c.1775del MANE Select ENSP00000339950.5:p.Asn592ThrfsTer?
ENST00000279227.9:c.1787del ENSP00000279227.5:p.Asn596ThrfsTer?
ENST00000345728.9:c.1775del ENSP00000339950.5:p.Asn592ThrfsTer?
ENST00000545896.1:c.338del ENSP00000440209.1:p.Asn113ThrfsTer?
NM_031471.5:c.1775del NP_113659.3:p.Asn592ThrfsTer?
NM_178443.2:c.1787del , LRG_180t1:c.1787del NP_848537.1:p.Asn596ThrfsTer?
XM_011545294.1:c.1787del XP_011543596.1:p.Asn596ThrfsTer?
XM_011545295.1:c.1247del XP_011543597.1:p.Asn416ThrfsTer?
XM_011545296.1:c.1247del XP_011543598.1:p.Asn416ThrfsTer?
XM_011545294.3:c.1787del XP_011543596.1:p.Asn596ThrfsTer?
XM_011545295.2:c.1247del XP_011543597.1:p.Asn416ThrfsTer?
XM_017018398.2:c.1775del XP_016873887.1:p.Asn592ThrfsTer?
XM_017018399.1:c.1235del XP_016873888.1:p.Asn412ThrfsTer?
NM_031471.6:c.1775del MANE Select NP_113659.3:p.Asn592ThrfsTer?
NM_001382361.1:c.1775del NP_001369290.1:p.Asn592ThrfsTer?
NM_001382362.1:c.1787del NP_001369291.1:p.Asn596ThrfsTer?
NM_001382363.1:c.1235del NP_001369292.1:p.Asn412ThrfsTer?
NM_001382364.1:c.1247del NP_001369293.1:p.Asn416ThrfsTer?
NM_001382448.1:c.1775del NP_001369377.1:p.Asn592ThrfsTer?
NM_178443.3:c.1787del NP_848537.1:p.Asn596ThrfsTer?