Canonical Allele Identifier: CA349457411

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409153A>C (hg19) ; chr2:g.178544426A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544426A>C , CM000664.2:g.178544426A>C	GRCh38
NC_000002.11:g.179409153A>C , CM000664.1:g.179409153A>C	GRCh37
NC_000002.10:g.179117399A>C	NCBI36
NG_011618.3:g.291377T>G , LRG_391:g.291377T>G
NG_051363.1:g.26600A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88099T>G (TTN)	ENSP00000343764.6:p.Tyr29367Asp
ENST00000342175.11:c.69184T>G (TTN)	ENSP00000340554.6:p.Tyr23062Asp
ENST00000359218.10:c.68983T>G (TTN)	ENSP00000352154.5:p.Tyr22995Asp
ENST00000342175.10:c.69184T>G (TTN)	ENSP00000340554.6:p.Tyr23062Asp
ENST00000342992.10:c.88099T>G (TTN)	ENSP00000343764.6:p.Tyr29367Asp
ENST00000359218.9:c.68983T>G (TTN)	ENSP00000352154.5:p.Tyr22995Asp
ENST00000460472.6:c.68608T>G (TTN)	ENSP00000434586.1:p.Tyr22870Asp
ENST00000589042.5:c.95803T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr31935Asp
ENST00000591111.5:c.90880T>G (TTN)	ENSP00000465570.1:p.Tyr30294Asp
ENST00000615779.4:c.90880T>G (TTN)	ENSP00000483597.1:p.Tyr30294Asp
NM_001256850.1:c.90880T>G (TTN)	NP_001243779.1:p.Tyr30294Asp
NM_001267550.2:c.95803T>G (TTN) MANE Select	NP_001254479.2:p.Tyr31935Asp
NM_003319.4:c.68608T>G (TTN)	NP_003310.4:p.Tyr22870Asp
NM_133378.4:c.88099T>G (TTN)	NP_596869.4:p.Tyr29367Asp
NM_133432.3:c.68983T>G (TTN)	NP_597676.3:p.Tyr22995Asp
NM_133437.4:c.69184T>G (TTN)	NP_597681.4:p.Tyr23062Asp
NR_038271.1:n.446+20790A>C (TTN-AS1)
NR_038272.1:n.2043+2065A>C (TTN-AS1)
XM_011511729.1:c.94900T>G (TTN)	XP_011510031.1:p.Tyr31634Asp
XM_011511730.1:c.68794T>G (TTN)	XP_011510032.1:p.Tyr22932Asp
XM_011511731.1:c.68653T>G (TTN)	XP_011510033.1:p.Tyr22885Asp
XM_017004819.1:c.94696T>G (TTN)	XP_016860308.1:p.Tyr31566Asp
XM_017004820.1:c.90094T>G (TTN)	XP_016860309.1:p.Tyr30032Asp
XM_017004821.1:c.90091T>G (TTN)	XP_016860310.1:p.Tyr30031Asp
XM_017004822.1:c.87133T>G (TTN)	XP_016860311.1:p.Tyr29045Asp
XM_017004823.1:c.68749T>G (TTN)	XP_016860312.1:p.Tyr22917Asp
XM_024453094.1:c.90244T>G (TTN)	XP_024308862.1:p.Tyr30082Asp
XM_024453095.1:c.90241T>G (TTN)	XP_024308863.1:p.Tyr30081Asp
XM_024453096.1:c.89674T>G (TTN)	XP_024308864.1:p.Tyr29892Asp
XM_024453097.1:c.87016T>G (TTN)	XP_024308865.1:p.Tyr29006Asp
XM_024453098.1:c.86935T>G (TTN)	XP_024308866.1:p.Tyr28979Asp
XM_024453099.1:c.68698T>G (TTN)	XP_024308867.1:p.Tyr22900Asp
XM_024453100.1:c.58552T>G (TTN)	XP_024308868.1:p.Tyr19518Asp