Canonical Allele Identifier: CA349451081

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408639A>C (hg19) ; chr2:g.178543912A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543912A>C , CM000664.2:g.178543912A>C	GRCh38
NC_000002.11:g.179408639A>C , CM000664.1:g.179408639A>C	GRCh37
NC_000002.10:g.179116885A>C	NCBI36
NG_011618.3:g.291891T>G , LRG_391:g.291891T>G
NG_051363.1:g.26086A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88528T>G (TTN)	ENSP00000343764.6:p.Tyr29510Asp
ENST00000342175.11:c.69613T>G (TTN)	ENSP00000340554.6:p.Tyr23205Asp
ENST00000359218.10:c.69412T>G (TTN)	ENSP00000352154.5:p.Tyr23138Asp
ENST00000342175.10:c.69613T>G (TTN)	ENSP00000340554.6:p.Tyr23205Asp
ENST00000342992.10:c.88528T>G (TTN)	ENSP00000343764.6:p.Tyr29510Asp
ENST00000359218.9:c.69412T>G (TTN)	ENSP00000352154.5:p.Tyr23138Asp
ENST00000460472.6:c.69037T>G (TTN)	ENSP00000434586.1:p.Tyr23013Asp
ENST00000589042.5:c.96232T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr32078Asp
ENST00000591111.5:c.91309T>G (TTN)	ENSP00000465570.1:p.Tyr30437Asp
ENST00000615779.4:c.91309T>G (TTN)	ENSP00000483597.1:p.Tyr30437Asp
NM_001256850.1:c.91309T>G (TTN)	NP_001243779.1:p.Tyr30437Asp
NM_001267550.2:c.96232T>G (TTN) MANE Select	NP_001254479.2:p.Tyr32078Asp
NM_003319.4:c.69037T>G (TTN)	NP_003310.4:p.Tyr23013Asp
NM_133378.4:c.88528T>G (TTN)	NP_596869.4:p.Tyr29510Asp
NM_133432.3:c.69412T>G (TTN)	NP_597676.3:p.Tyr23138Asp
NM_133437.4:c.69613T>G (TTN)	NP_597681.4:p.Tyr23205Asp
NR_038271.1:n.446+20276A>C (TTN-AS1)
NR_038272.1:n.2043+1551A>C (TTN-AS1)
XM_011511729.1:c.95329T>G (TTN)	XP_011510031.1:p.Tyr31777Asp
XM_011511730.1:c.69223T>G (TTN)	XP_011510032.1:p.Tyr23075Asp
XM_011511731.1:c.69082T>G (TTN)	XP_011510033.1:p.Tyr23028Asp
XM_017004819.1:c.95125T>G (TTN)	XP_016860308.1:p.Tyr31709Asp
XM_017004820.1:c.90523T>G (TTN)	XP_016860309.1:p.Tyr30175Asp
XM_017004821.1:c.90520T>G (TTN)	XP_016860310.1:p.Tyr30174Asp
XM_017004822.1:c.87562T>G (TTN)	XP_016860311.1:p.Tyr29188Asp
XM_017004823.1:c.69178T>G (TTN)	XP_016860312.1:p.Tyr23060Asp
XM_024453094.1:c.90673T>G (TTN)	XP_024308862.1:p.Tyr30225Asp
XM_024453095.1:c.90670T>G (TTN)	XP_024308863.1:p.Tyr30224Asp
XM_024453096.1:c.90103T>G (TTN)	XP_024308864.1:p.Tyr30035Asp
XM_024453097.1:c.87445T>G (TTN)	XP_024308865.1:p.Tyr29149Asp
XM_024453098.1:c.87364T>G (TTN)	XP_024308866.1:p.Tyr29122Asp
XM_024453099.1:c.69127T>G (TTN)	XP_024308867.1:p.Tyr23043Asp
XM_024453100.1:c.58981T>G (TTN)	XP_024308868.1:p.Tyr19661Asp