Canonical Allele Identifier: CA645528607

Gene: TTN TTN-AS1

Linked Data

• COSMIC: COSM4748100 ; COSM4748101 ; COSM4748102 ; COSM4748103

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543881del , CM000664.2:g.178543881del	GRCh38
NC_000002.11:g.179408608del , CM000664.1:g.179408608del	GRCh37
NC_000002.10:g.179116854del	NCBI36
NG_011618.3:g.291925del , LRG_391:g.291925del
NG_051363.1:g.26055del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88562del (TTN)	ENSP00000343764.6:p.Asn29521ThrfsTer24
ENST00000342175.11:c.69647del (TTN)	ENSP00000340554.6:p.Asn23216ThrfsTer24
ENST00000359218.10:c.69446del (TTN)	ENSP00000352154.5:p.Asn23149ThrfsTer24
ENST00000342175.10:c.69647del (TTN)	ENSP00000340554.6:p.Asn23216ThrfsTer24
ENST00000342992.10:c.88562del (TTN)	ENSP00000343764.6:p.Asn29521ThrfsTer24
ENST00000359218.9:c.69446del (TTN)	ENSP00000352154.5:p.Asn23149ThrfsTer24
ENST00000460472.6:c.69071del (TTN)	ENSP00000434586.1:p.Asn23024ThrfsTer24
ENST00000589042.5:c.96266del (TTN) MANE Select	ENSP00000467141.1:p.Asn32089ThrfsTer24
ENST00000591111.5:c.91343del (TTN)	ENSP00000465570.1:p.Asn30448ThrfsTer24
ENST00000615779.4:c.91343del (TTN)	ENSP00000483597.1:p.Asn30448ThrfsTer24
NM_001256850.1:c.91343del (TTN)	NP_001243779.1:p.Asn30448ThrfsTer24
NM_001267550.2:c.96266del (TTN) MANE Select	NP_001254479.2:p.Asn32089ThrfsTer24
NM_003319.4:c.69071del (TTN)	NP_003310.4:p.Asn23024ThrfsTer24
NM_133378.4:c.88562del (TTN)	NP_596869.4:p.Asn29521ThrfsTer24
NM_133432.3:c.69446del (TTN)	NP_597676.3:p.Asn23149ThrfsTer24
NM_133437.4:c.69647del (TTN)	NP_597681.4:p.Asn23216ThrfsTer24
NR_038271.1:n.446+20245del (TTN-AS1)
NR_038272.1:n.2043+1520del (TTN-AS1)
XM_011511729.1:c.95363del (TTN)	XP_011510031.1:p.Asn31788ThrfsTer24
XM_011511730.1:c.69257del (TTN)	XP_011510032.1:p.Asn23086ThrfsTer24
XM_011511731.1:c.69116del (TTN)	XP_011510033.1:p.Asn23039ThrfsTer24
XM_017004819.1:c.95159del (TTN)	XP_016860308.1:p.Asn31720ThrfsTer24
XM_017004820.1:c.90557del (TTN)	XP_016860309.1:p.Asn30186ThrfsTer24
XM_017004821.1:c.90554del (TTN)	XP_016860310.1:p.Asn30185ThrfsTer24
XM_017004822.1:c.87596del (TTN)	XP_016860311.1:p.Asn29199ThrfsTer24
XM_017004823.1:c.69212del (TTN)	XP_016860312.1:p.Asn23071ThrfsTer24
XM_024453094.1:c.90707del (TTN)	XP_024308862.1:p.Asn30236ThrfsTer24
XM_024453095.1:c.90704del (TTN)	XP_024308863.1:p.Asn30235ThrfsTer24
XM_024453096.1:c.90137del (TTN)	XP_024308864.1:p.Asn30046ThrfsTer24
XM_024453097.1:c.87479del (TTN)	XP_024308865.1:p.Asn29160ThrfsTer24
XM_024453098.1:c.87398del (TTN)	XP_024308866.1:p.Asn29133ThrfsTer24
XM_024453099.1:c.69161del (TTN)	XP_024308867.1:p.Asn23054ThrfsTer24
XM_024453100.1:c.59015del (TTN)	XP_024308868.1:p.Asn19672ThrfsTer24