Canonical Allele Identifier: CA349621779

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179435273T>G (hg19) ; chr2:g.178570546T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570546T>G , CM000664.2:g.178570546T>G	GRCh38
NC_000002.11:g.179435273T>G , CM000664.1:g.179435273T>G	GRCh37
NC_000002.10:g.179143519T>G	NCBI36
NG_011618.3:g.265257A>C , LRG_391:g.265257A>C
NG_051363.1:g.52720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.67882A>C (TTN)	ENSP00000343764.6:p.Thr22628Pro
ENST00000342175.11:c.48967A>C (TTN)	ENSP00000340554.6:p.Thr16323Pro
ENST00000359218.10:c.48766A>C (TTN)	ENSP00000352154.5:p.Thr16256Pro
ENST00000342175.10:c.48967A>C (TTN)	ENSP00000340554.6:p.Thr16323Pro
ENST00000342992.10:c.67882A>C (TTN)	ENSP00000343764.6:p.Thr22628Pro
ENST00000359218.9:c.48766A>C (TTN)	ENSP00000352154.5:p.Thr16256Pro
ENST00000460472.6:c.48391A>C (TTN)	ENSP00000434586.1:p.Thr16131Pro
ENST00000589042.5:c.75586A>C (TTN) MANE Select	ENSP00000467141.1:p.Thr25196Pro
ENST00000591111.5:c.70663A>C (TTN)	ENSP00000465570.1:p.Thr23555Pro
ENST00000615779.4:c.70663A>C (TTN)	ENSP00000483597.1:p.Thr23555Pro
NM_001256850.1:c.70663A>C (TTN)	NP_001243779.1:p.Thr23555Pro
NM_001267550.2:c.75586A>C (TTN) MANE Select	NP_001254479.2:p.Thr25196Pro
NM_003319.4:c.48391A>C (TTN)	NP_003310.4:p.Thr16131Pro
NM_133378.4:c.67882A>C (TTN)	NP_596869.4:p.Thr22628Pro
NM_133432.3:c.48766A>C (TTN)	NP_597676.3:p.Thr16256Pro
NM_133437.4:c.48967A>C (TTN)	NP_597681.4:p.Thr16323Pro
NR_038271.1:n.447-754T>G (TTN-AS1)
NR_038272.1:n.2044-12026T>G (TTN-AS1)
XM_011511729.1:c.74683A>C (TTN)	XP_011510031.1:p.Thr24895Pro
XM_011511730.1:c.48577A>C (TTN)	XP_011510032.1:p.Thr16193Pro
XM_011511731.1:c.48436A>C (TTN)	XP_011510033.1:p.Thr16146Pro
XM_017004819.1:c.74479A>C (TTN)	XP_016860308.1:p.Thr24827Pro
XM_017004820.1:c.69877A>C (TTN)	XP_016860309.1:p.Thr23293Pro
XM_017004821.1:c.69874A>C (TTN)	XP_016860310.1:p.Thr23292Pro
XM_017004822.1:c.66916A>C (TTN)	XP_016860311.1:p.Thr22306Pro
XM_017004823.1:c.48532A>C (TTN)	XP_016860312.1:p.Thr16178Pro
XM_024453094.1:c.70027A>C (TTN)	XP_024308862.1:p.Thr23343Pro
XM_024453095.1:c.70024A>C (TTN)	XP_024308863.1:p.Thr23342Pro
XM_024453096.1:c.69457A>C (TTN)	XP_024308864.1:p.Thr23153Pro
XM_024453097.1:c.66799A>C (TTN)	XP_024308865.1:p.Thr22267Pro
XM_024453098.1:c.66718A>C (TTN)	XP_024308866.1:p.Thr22240Pro
XM_024453099.1:c.48481A>C (TTN)	XP_024308867.1:p.Thr16161Pro
XM_024453100.1:c.38335A>C (TTN)	XP_024308868.1:p.Thr12779Pro