Canonical Allele Identifier: CA349601160

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178612963A>C , CM000664.2:g.178612963A>C	GRCh38
NC_000002.11:g.179477690A>C , CM000664.1:g.179477690A>C	GRCh37
NC_000002.10:g.179185935A>C	NCBI36
NG_011618.3:g.222840T>G , LRG_391:g.222840T>G
NG_051363.1:g.95137A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.49758T>G (TTN) MANE Select	NP_001254479.2:p.Tyr16586Ter
ENST00000589042.5:c.49758T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr16586Ter
NM_001256850.1:c.44835T>G (TTN)	NP_001243779.1:p.Tyr14945Ter
NM_003319.4:c.22563T>G (TTN)	NP_003310.4:p.Tyr7521Ter
NM_133378.4:c.42054T>G (TTN)	NP_596869.4:p.Tyr14018Ter
NM_133432.3:c.22938T>G (TTN)	NP_597676.3:p.Tyr7646Ter
NM_133437.4:c.23139T>G (TTN)	NP_597681.4:p.Tyr7713Ter
NR_038271.1:n.783-1072A>C (TTN-AS1)
ENST00000342175.10:c.23139T>G (TTN)	ENSP00000340554.6:p.Tyr7713Ter
ENST00000342175.11:c.23139T>G (TTN)	ENSP00000340554.6:p.Tyr7713Ter
ENST00000342992.10:c.42054T>G (TTN)	ENSP00000343764.6:p.Tyr14018Ter
ENST00000342992.11:c.42054T>G (TTN)	ENSP00000343764.6:p.Tyr14018Ter
ENST00000359218.10:c.22938T>G (TTN)	ENSP00000352154.5:p.Tyr7646Ter
ENST00000359218.9:c.22938T>G (TTN)	ENSP00000352154.5:p.Tyr7646Ter
ENST00000460472.6:c.22563T>G (TTN)	ENSP00000434586.1:p.Tyr7521Ter
ENST00000591111.5:c.44835T>G (TTN)	ENSP00000465570.1:p.Tyr14945Ter
ENST00000615779.4:c.44835T>G (TTN)	ENSP00000483597.1:p.Tyr14945Ter
XM_011511729.1:c.48855T>G (TTN)	XP_011510031.1:p.Tyr16285Ter
XM_011511730.1:c.22749T>G (TTN)	XP_011510032.1:p.Tyr7583Ter
XM_011511731.1:c.22608T>G (TTN)	XP_011510033.1:p.Tyr7536Ter
XM_017004819.1:c.48651T>G (TTN)	XP_016860308.1:p.Tyr16217Ter
XM_017004820.1:c.44049T>G (TTN)	XP_016860309.1:p.Tyr14683Ter
XM_017004821.1:c.44046T>G (TTN)	XP_016860310.1:p.Tyr14682Ter
XM_017004822.1:c.41088T>G (TTN)	XP_016860311.1:p.Tyr13696Ter
XM_017004823.1:c.22704T>G (TTN)	XP_016860312.1:p.Tyr7568Ter
XM_024453094.1:c.44199T>G (TTN)	XP_024308862.1:p.Tyr14733Ter
XM_024453095.1:c.44196T>G (TTN)	XP_024308863.1:p.Tyr14732Ter
XM_024453096.1:c.43629T>G (TTN)	XP_024308864.1:p.Tyr14543Ter
XM_024453097.1:c.40971T>G (TTN)	XP_024308865.1:p.Tyr13657Ter
XM_024453098.1:c.40890T>G (TTN)	XP_024308866.1:p.Tyr13630Ter
XM_024453099.1:c.22653T>G (TTN)	XP_024308867.1:p.Tyr7551Ter
XM_024453100.1:c.12507T>G (TTN)	XP_024308868.1:p.Tyr4169Ter