Canonical Allele Identifier: CA1310521542

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544360A= , CM000664.2:g.178544360A=	GRCh38
NC_000002.11:g.179409087A= , CM000664.1:g.179409087A=	GRCh37
NC_000002.10:g.179117333A=	NCBI36
NG_011618.3:g.291443T= , LRG_391:g.291443T=
NG_051363.1:g.26534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88165T= (TTN)	ENSP00000343764.6:p.Tyr29389=
ENST00000342175.11:c.69250T= (TTN)	ENSP00000340554.6:p.Tyr23084=
ENST00000359218.10:c.69049T= (TTN)	ENSP00000352154.5:p.Tyr23017=
ENST00000342175.10:c.69250T= (TTN)	ENSP00000340554.6:p.Tyr23084=
ENST00000342992.10:c.88165T= (TTN)	ENSP00000343764.6:p.Tyr29389=
ENST00000359218.9:c.69049T= (TTN)	ENSP00000352154.5:p.Tyr23017=
ENST00000460472.6:c.68674T= (TTN)	ENSP00000434586.1:p.Tyr22892=
ENST00000589042.5:c.95869T= (TTN) MANE Select	ENSP00000467141.1:p.Tyr31957=
ENST00000591111.5:c.90946T= (TTN)	ENSP00000465570.1:p.Tyr30316=
ENST00000615779.4:c.90946T= (TTN)	ENSP00000483597.1:p.Tyr30316=
NM_001256850.1:c.90946T= (TTN)	NP_001243779.1:p.Tyr30316=
NM_001267550.2:c.95869T= (TTN) MANE Select	NP_001254479.2:p.Tyr31957=
NM_003319.4:c.68674T= (TTN)	NP_003310.4:p.Tyr22892=
NM_133378.4:c.88165T= (TTN)	NP_596869.4:p.Tyr29389=
NM_133432.3:c.69049T= (TTN)	NP_597676.3:p.Tyr23017=
NM_133437.4:c.69250T= (TTN)	NP_597681.4:p.Tyr23084=
NR_038271.1:n.446+20724A= (TTN-AS1)
NR_038272.1:n.2043+1999A= (TTN-AS1)
XM_011511729.1:c.94966T= (TTN)	XP_011510031.1:p.Tyr31656=
XM_011511730.1:c.68860T= (TTN)	XP_011510032.1:p.Tyr22954=
XM_011511731.1:c.68719T= (TTN)	XP_011510033.1:p.Tyr22907=
XM_017004819.1:c.94762T= (TTN)	XP_016860308.1:p.Tyr31588=
XM_017004820.1:c.90160T= (TTN)	XP_016860309.1:p.Tyr30054=
XM_017004821.1:c.90157T= (TTN)	XP_016860310.1:p.Tyr30053=
XM_017004822.1:c.87199T= (TTN)	XP_016860311.1:p.Tyr29067=
XM_017004823.1:c.68815T= (TTN)	XP_016860312.1:p.Tyr22939=
XM_024453094.1:c.90310T= (TTN)	XP_024308862.1:p.Tyr30104=
XM_024453095.1:c.90307T= (TTN)	XP_024308863.1:p.Tyr30103=
XM_024453096.1:c.89740T= (TTN)	XP_024308864.1:p.Tyr29914=
XM_024453097.1:c.87082T= (TTN)	XP_024308865.1:p.Tyr29028=
XM_024453098.1:c.87001T= (TTN)	XP_024308866.1:p.Tyr29001=
XM_024453099.1:c.68764T= (TTN)	XP_024308867.1:p.Tyr22922=
XM_024453100.1:c.58618T= (TTN)	XP_024308868.1:p.Tyr19540=