Canonical Allele Identifier: CA349454569

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178588137A>C , CM000664.2:g.178588137A>C	GRCh38
NC_000002.11:g.179452864A>C , CM000664.1:g.179452864A>C	GRCh37
NC_000002.10:g.179161110A>C	NCBI36
NG_011618.3:g.247666T>G , LRG_391:g.247666T>G
NG_051363.1:g.70311A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.63270T>G (TTN) MANE Select	NP_001254479.2:p.Tyr21090Ter
ENST00000589042.5:c.63270T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr21090Ter
NM_001256850.1:c.58347T>G (TTN)	NP_001243779.1:p.Tyr19449Ter
NM_003319.4:c.36075T>G (TTN)	NP_003310.4:p.Tyr12025Ter
NM_133378.4:c.55566T>G (TTN)	NP_596869.4:p.Tyr18522Ter
NM_133432.3:c.36450T>G (TTN)	NP_597676.3:p.Tyr12150Ter
NM_133437.4:c.36651T>G (TTN)	NP_597681.4:p.Tyr12217Ter
NR_038271.1:n.597-9459A>C (TTN-AS1)
NR_038272.1:n.3189-3002A>C (TTN-AS1)
ENST00000342175.10:c.36651T>G (TTN)	ENSP00000340554.6:p.Tyr12217Ter
ENST00000342175.11:c.36651T>G (TTN)	ENSP00000340554.6:p.Tyr12217Ter
ENST00000342992.10:c.55566T>G (TTN)	ENSP00000343764.6:p.Tyr18522Ter
ENST00000342992.11:c.55566T>G (TTN)	ENSP00000343764.6:p.Tyr18522Ter
ENST00000359218.10:c.36450T>G (TTN)	ENSP00000352154.5:p.Tyr12150Ter
ENST00000359218.9:c.36450T>G (TTN)	ENSP00000352154.5:p.Tyr12150Ter
ENST00000460472.6:c.36075T>G (TTN)	ENSP00000434586.1:p.Tyr12025Ter
ENST00000591111.5:c.58347T>G (TTN)	ENSP00000465570.1:p.Tyr19449Ter
ENST00000615779.4:c.58347T>G (TTN)	ENSP00000483597.1:p.Tyr19449Ter
XM_011511729.1:c.62367T>G (TTN)	XP_011510031.1:p.Tyr20789Ter
XM_011511730.1:c.36261T>G (TTN)	XP_011510032.1:p.Tyr12087Ter
XM_011511731.1:c.36120T>G (TTN)	XP_011510033.1:p.Tyr12040Ter
XM_017004819.1:c.62163T>G (TTN)	XP_016860308.1:p.Tyr20721Ter
XM_017004820.1:c.57561T>G (TTN)	XP_016860309.1:p.Tyr19187Ter
XM_017004821.1:c.57558T>G (TTN)	XP_016860310.1:p.Tyr19186Ter
XM_017004822.1:c.54600T>G (TTN)	XP_016860311.1:p.Tyr18200Ter
XM_017004823.1:c.36216T>G (TTN)	XP_016860312.1:p.Tyr12072Ter
XM_024453094.1:c.57711T>G (TTN)	XP_024308862.1:p.Tyr19237Ter
XM_024453095.1:c.57708T>G (TTN)	XP_024308863.1:p.Tyr19236Ter
XM_024453096.1:c.57141T>G (TTN)	XP_024308864.1:p.Tyr19047Ter
XM_024453097.1:c.54483T>G (TTN)	XP_024308865.1:p.Tyr18161Ter
XM_024453098.1:c.54402T>G (TTN)	XP_024308866.1:p.Tyr18134Ter
XM_024453099.1:c.36165T>G (TTN)	XP_024308867.1:p.Tyr12055Ter
XM_024453100.1:c.26019T>G (TTN)	XP_024308868.1:p.Tyr8673Ter