Canonical Allele Identifier: CA645528354

Gene: TTN TTN-AS1

Linked Data

• COSMIC: COSM4582909 ; COSM4582910 ; COSM4582911 ; COSM4582912

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178590905_178590907del , CM000664.2:g.178590905_178590907del	GRCh38
NC_000002.11:g.179455632_179455634del , CM000664.1:g.179455632_179455634del	GRCh37
NC_000002.10:g.179163878_179163880del	NCBI36
NG_011618.3:g.244901_244903del , LRG_391:g.244901_244903del
NG_051363.1:g.73079_73081del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.53119_53121del (TTN)	ENSP00000343764.6:p.Pro17707del
ENST00000342175.11:c.34204_34206del (TTN)	ENSP00000340554.6:p.Pro11402del
ENST00000359218.10:c.34003_34005del (TTN)	ENSP00000352154.5:p.Pro11335del
ENST00000342175.10:c.34204_34206del (TTN)	ENSP00000340554.6:p.Pro11402del
ENST00000342992.10:c.53119_53121del (TTN)	ENSP00000343764.6:p.Pro17707del
ENST00000359218.9:c.34003_34005del (TTN)	ENSP00000352154.5:p.Pro11335del
ENST00000460472.6:c.33628_33630del (TTN)	ENSP00000434586.1:p.Pro11210del
ENST00000589042.5:c.60823_60825del (TTN) MANE Select	ENSP00000467141.1:p.Pro20275del
ENST00000591111.5:c.55900_55902del (TTN)	ENSP00000465570.1:p.Pro18634del
ENST00000615779.4:c.55900_55902del (TTN)	ENSP00000483597.1:p.Pro18634del
NM_001256850.1:c.55900_55902del (TTN)	NP_001243779.1:p.Pro18634del
NM_001267550.2:c.60823_60825del (TTN) MANE Select	NP_001254479.2:p.Pro20275del
NM_003319.4:c.33628_33630del (TTN)	NP_003310.4:p.Pro11210del
NM_133378.4:c.53119_53121del (TTN)	NP_596869.4:p.Pro17707del
NM_133432.3:c.34003_34005del (TTN)	NP_597676.3:p.Pro11335del
NM_133437.4:c.34204_34206del (TTN)	NP_597681.4:p.Pro11402del
NR_038271.1:n.597-6691_597-6689del (TTN-AS1)
NR_038272.1:n.3189-234_3189-232del (TTN-AS1)
XM_011511729.1:c.59920_59922del (TTN)	XP_011510031.1:p.Pro19974del
XM_011511730.1:c.33814_33816del (TTN)	XP_011510032.1:p.Pro11272del
XM_011511731.1:c.33673_33675del (TTN)	XP_011510033.1:p.Pro11225del
XM_017004819.1:c.59716_59718del (TTN)	XP_016860308.1:p.Pro19906del
XM_017004820.1:c.55114_55116del (TTN)	XP_016860309.1:p.Pro18372del
XM_017004821.1:c.55111_55113del (TTN)	XP_016860310.1:p.Pro18371del
XM_017004822.1:c.52153_52155del (TTN)	XP_016860311.1:p.Pro17385del
XM_017004823.1:c.33769_33771del (TTN)	XP_016860312.1:p.Pro11257del
XM_024453094.1:c.55264_55266del (TTN)	XP_024308862.1:p.Pro18422del
XM_024453095.1:c.55261_55263del (TTN)	XP_024308863.1:p.Pro18421del
XM_024453096.1:c.54694_54696del (TTN)	XP_024308864.1:p.Pro18232del
XM_024453097.1:c.52036_52038del (TTN)	XP_024308865.1:p.Pro17346del
XM_024453098.1:c.51955_51957del (TTN)	XP_024308866.1:p.Pro17319del
XM_024453099.1:c.33718_33720del (TTN)	XP_024308867.1:p.Pro11240del
XM_024453100.1:c.23572_23574del (TTN)	XP_024308868.1:p.Pro7858del