Canonical Allele Identifier: CA1310540503

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591979_178591998delinsGAGAGGATCCAAAGCCTTGA , CM000664.2:g.178591979_178591998delinsGAGAGGATCCAAAGCCTTGA	GRCh38
NC_000002.11:g.179456706_179456725delinsGAGAGGATCCAAAGCCTTGA , CM000664.1:g.179456706_179456725delinsGAGAGGATCCAAAGCCTTGA	GRCh37
NC_000002.10:g.179164952_179164971delinsGAGAGGATCCAAAGCCTTGA	NCBI36
NG_011618.3:g.243805_243824delinsTCAAGGCTTTGGATCCTCTC , LRG_391:g.243805_243824delinsTCAAGGCTTTGGATCCTCTC
NG_051363.1:g.74153_74172delinsGAGAGGATCCAAAGCCTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52202_52221delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000343764.6:p.Ile17401=
ENST00000342175.11:c.33287_33306delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000340554.6:p.Ile11096=
ENST00000359218.10:c.33086_33105delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000352154.5:p.Ile11029=
ENST00000342175.10:c.33287_33306delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000340554.6:p.Ile11096=
ENST00000342992.10:c.52202_52221delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000343764.6:p.Ile17401=
ENST00000359218.9:c.33086_33105delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000352154.5:p.Ile11029=
ENST00000460472.6:c.32711_32730delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000434586.1:p.Ile10904=
ENST00000589042.5:c.59906_59925delinsTCAAGGCTTTGGATCCTCTC (TTN) MANE Select	ENSP00000467141.1:p.Ile19969=
ENST00000591111.5:c.54983_55002delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000465570.1:p.Ile18328=
ENST00000615779.4:c.54983_55002delinsTCAAGGCTTTGGATCCTCTC (TTN)	ENSP00000483597.1:p.Ile18328=
NM_001256850.1:c.54983_55002delinsTCAAGGCTTTGGATCCTCTC (TTN)	NP_001243779.1:p.Ile18328=
NM_001267550.2:c.59906_59925delinsTCAAGGCTTTGGATCCTCTC (TTN) MANE Select	NP_001254479.2:p.Ile19969=
NM_003319.4:c.32711_32730delinsTCAAGGCTTTGGATCCTCTC (TTN)	NP_003310.4:p.Ile10904=
NM_133378.4:c.52202_52221delinsTCAAGGCTTTGGATCCTCTC (TTN)	NP_596869.4:p.Ile17401=
NM_133432.3:c.33086_33105delinsTCAAGGCTTTGGATCCTCTC (TTN)	NP_597676.3:p.Ile11029=
NM_133437.4:c.33287_33306delinsTCAAGGCTTTGGATCCTCTC (TTN)	NP_597681.4:p.Ile11096=
NR_038271.1:n.597-5617_597-5598delinsGAGAGGATCCAAAGCCTTGA (TTN-AS1)
NR_038272.1:n.3364+665_3364+684delinsGAGAGGATCCAAAGCCTTGA (TTN-AS1)
XM_011511729.1:c.59003_59022delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_011510031.1:p.Ile19668=
XM_011511730.1:c.32897_32916delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_011510032.1:p.Ile10966=
XM_011511731.1:c.32756_32775delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_011510033.1:p.Ile10919=
XM_017004819.1:c.58799_58818delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_016860308.1:p.Ile19600=
XM_017004820.1:c.54197_54216delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_016860309.1:p.Ile18066=
XM_017004821.1:c.54194_54213delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_016860310.1:p.Ile18065=
XM_017004822.1:c.51236_51255delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_016860311.1:p.Ile17079=
XM_017004823.1:c.32852_32871delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_016860312.1:p.Ile10951=
XM_024453094.1:c.54347_54366delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308862.1:p.Ile18116=
XM_024453095.1:c.54344_54363delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308863.1:p.Ile18115=
XM_024453096.1:c.53777_53796delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308864.1:p.Ile17926=
XM_024453097.1:c.51119_51138delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308865.1:p.Ile17040=
XM_024453098.1:c.51038_51057delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308866.1:p.Ile17013=
XM_024453099.1:c.32801_32820delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308867.1:p.Ile10934=
XM_024453100.1:c.22655_22674delinsTCAAGGCTTTGGATCCTCTC (TTN)	XP_024308868.1:p.Ile7552=