Canonical Allele Identifier: CA1310540018

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178592728_178592729delinsCA , CM000664.2:g.178592728_178592729delinsCA	GRCh38
NC_000002.11:g.179457455_179457456delinsCA , CM000664.1:g.179457455_179457456delinsCA	GRCh37
NC_000002.10:g.179165701_179165702delinsCA	NCBI36
NG_011618.3:g.243074_243075delinsTG , LRG_391:g.243074_243075delinsTG
NG_051363.1:g.74902_74903delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51640+46_51640+47delinsTG (TTN)	ENSP00000343764.6:n.51640+46_51640+47delinsTG
ENST00000342175.11:c.32725+46_32725+47delinsTG (TTN)	ENSP00000340554.6:n.32725+46_32725+47delinsTG
ENST00000359218.10:c.32524+46_32524+47delinsTG (TTN)	ENSP00000352154.5:n.32524+46_32524+47delinsTG
ENST00000342175.10:c.32725+46_32725+47delinsTG (TTN)	ENSP00000340554.6:n.32725+46_32725+47delinsTG
ENST00000342992.10:c.51640+46_51640+47delinsTG (TTN)	ENSP00000343764.6:n.51640+46_51640+47delinsTG
ENST00000359218.9:c.32524+46_32524+47delinsTG (TTN)	ENSP00000352154.5:n.32524+46_32524+47delinsTG
ENST00000460472.6:c.32149+46_32149+47delinsTG (TTN)	ENSP00000434586.1:n.32149+46_32149+47delinsTG
ENST00000589042.5:c.59344+46_59344+47delinsTG (TTN) MANE Select	ENSP00000467141.1:n.59344+46_59344+47delinsTG
ENST00000591111.5:c.54421+46_54421+47delinsTG (TTN)	ENSP00000465570.1:n.54421+46_54421+47delinsTG
ENST00000615779.4:c.54421+46_54421+47delinsTG (TTN)	ENSP00000483597.1:n.54421+46_54421+47delinsTG
NM_001256850.1:c.54421+46_54421+47delinsTG (TTN)	NP_001243779.1:n.54421+46_54421+47delinsTG
NM_001267550.2:c.59344+46_59344+47delinsTG (TTN) MANE Select	NP_001254479.2:n.59344+46_59344+47delinsTG
NM_003319.4:c.32149+46_32149+47delinsTG (TTN)	NP_003310.4:n.32149+46_32149+47delinsTG
NM_133378.4:c.51640+46_51640+47delinsTG (TTN)	NP_596869.4:n.51640+46_51640+47delinsTG
NM_133432.3:c.32524+46_32524+47delinsTG (TTN)	NP_597676.3:n.32524+46_32524+47delinsTG
NM_133437.4:c.32725+46_32725+47delinsTG (TTN)	NP_597681.4:n.32725+46_32725+47delinsTG
NR_038271.1:n.597-4868_597-4867delinsCA (TTN-AS1)
NR_038272.1:n.3364+1414_3364+1415delinsCA (TTN-AS1)
XM_011511729.1:c.58441+46_58441+47delinsTG (TTN)	XP_011510031.1:n.58441+46_58441+47delinsTG
XM_011511730.1:c.32335+46_32335+47delinsTG (TTN)	XP_011510032.1:n.32335+46_32335+47delinsTG
XM_011511731.1:c.32194+46_32194+47delinsTG (TTN)	XP_011510033.1:n.32194+46_32194+47delinsTG
XM_017004819.1:c.58237+46_58237+47delinsTG (TTN)	XP_016860308.1:n.58237+46_58237+47delinsTG
XM_017004820.1:c.53635+46_53635+47delinsTG (TTN)	XP_016860309.1:n.53635+46_53635+47delinsTG
XM_017004821.1:c.53632+46_53632+47delinsTG (TTN)	XP_016860310.1:n.53632+46_53632+47delinsTG
XM_017004822.1:c.50674+46_50674+47delinsTG (TTN)	XP_016860311.1:n.50674+46_50674+47delinsTG
XM_017004823.1:c.32290+46_32290+47delinsTG (TTN)	XP_016860312.1:n.32290+46_32290+47delinsTG
XM_024453094.1:c.53785+46_53785+47delinsTG (TTN)	XP_024308862.1:n.53785+46_53785+47delinsTG
XM_024453095.1:c.53782+46_53782+47delinsTG (TTN)	XP_024308863.1:n.53782+46_53782+47delinsTG
XM_024453096.1:c.53215+46_53215+47delinsTG (TTN)	XP_024308864.1:n.53215+46_53215+47delinsTG
XM_024453097.1:c.50557+46_50557+47delinsTG (TTN)	XP_024308865.1:n.50557+46_50557+47delinsTG
XM_024453098.1:c.50476+46_50476+47delinsTG (TTN)	XP_024308866.1:n.50476+46_50476+47delinsTG
XM_024453099.1:c.32239+46_32239+47delinsTG (TTN)	XP_024308867.1:n.32239+46_32239+47delinsTG
XM_024453100.1:c.22093+46_22093+47delinsTG (TTN)	XP_024308868.1:n.22093+46_22093+47delinsTG