Canonical Allele Identifier: CA349456570

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409086T>C (hg19) ; chr2:g.178544359T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544359T>C , CM000664.2:g.178544359T>C	GRCh38
NC_000002.11:g.179409086T>C , CM000664.1:g.179409086T>C	GRCh37
NC_000002.10:g.179117332T>C	NCBI36
NG_011618.3:g.291444A>G , LRG_391:g.291444A>G
NG_051363.1:g.26533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88166A>G (TTN)	ENSP00000343764.6:p.Tyr29389Cys
ENST00000342175.11:c.69251A>G (TTN)	ENSP00000340554.6:p.Tyr23084Cys
ENST00000359218.10:c.69050A>G (TTN)	ENSP00000352154.5:p.Tyr23017Cys
ENST00000342175.10:c.69251A>G (TTN)	ENSP00000340554.6:p.Tyr23084Cys
ENST00000342992.10:c.88166A>G (TTN)	ENSP00000343764.6:p.Tyr29389Cys
ENST00000359218.9:c.69050A>G (TTN)	ENSP00000352154.5:p.Tyr23017Cys
ENST00000460472.6:c.68675A>G (TTN)	ENSP00000434586.1:p.Tyr22892Cys
ENST00000589042.5:c.95870A>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr31957Cys
ENST00000591111.5:c.90947A>G (TTN)	ENSP00000465570.1:p.Tyr30316Cys
ENST00000615779.4:c.90947A>G (TTN)	ENSP00000483597.1:p.Tyr30316Cys
NM_001256850.1:c.90947A>G (TTN)	NP_001243779.1:p.Tyr30316Cys
NM_001267550.2:c.95870A>G (TTN) MANE Select	NP_001254479.2:p.Tyr31957Cys
NM_003319.4:c.68675A>G (TTN)	NP_003310.4:p.Tyr22892Cys
NM_133378.4:c.88166A>G (TTN)	NP_596869.4:p.Tyr29389Cys
NM_133432.3:c.69050A>G (TTN)	NP_597676.3:p.Tyr23017Cys
NM_133437.4:c.69251A>G (TTN)	NP_597681.4:p.Tyr23084Cys
NR_038271.1:n.446+20723T>C (TTN-AS1)
NR_038272.1:n.2043+1998T>C (TTN-AS1)
XM_011511729.1:c.94967A>G (TTN)	XP_011510031.1:p.Tyr31656Cys
XM_011511730.1:c.68861A>G (TTN)	XP_011510032.1:p.Tyr22954Cys
XM_011511731.1:c.68720A>G (TTN)	XP_011510033.1:p.Tyr22907Cys
XM_017004819.1:c.94763A>G (TTN)	XP_016860308.1:p.Tyr31588Cys
XM_017004820.1:c.90161A>G (TTN)	XP_016860309.1:p.Tyr30054Cys
XM_017004821.1:c.90158A>G (TTN)	XP_016860310.1:p.Tyr30053Cys
XM_017004822.1:c.87200A>G (TTN)	XP_016860311.1:p.Tyr29067Cys
XM_017004823.1:c.68816A>G (TTN)	XP_016860312.1:p.Tyr22939Cys
XM_024453094.1:c.90311A>G (TTN)	XP_024308862.1:p.Tyr30104Cys
XM_024453095.1:c.90308A>G (TTN)	XP_024308863.1:p.Tyr30103Cys
XM_024453096.1:c.89741A>G (TTN)	XP_024308864.1:p.Tyr29914Cys
XM_024453097.1:c.87083A>G (TTN)	XP_024308865.1:p.Tyr29028Cys
XM_024453098.1:c.87002A>G (TTN)	XP_024308866.1:p.Tyr29001Cys
XM_024453099.1:c.68765A>G (TTN)	XP_024308867.1:p.Tyr22922Cys
XM_024453100.1:c.58619A>G (TTN)	XP_024308868.1:p.Tyr19540Cys