Canonical Allele Identifier: CA349407065

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395257G>T (hg19) ; chr2:g.178530530G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530530G>T , CM000664.2:g.178530530G>T	GRCh38
NC_000002.11:g.179395257G>T , CM000664.1:g.179395257G>T	GRCh37
NC_000002.10:g.179103503G>T	NCBI36
NG_011618.3:g.305273C>A , LRG_391:g.305273C>A
NG_051363.1:g.12704G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98381C>A (TTN)	ENSP00000343764.6:p.Ser32794Tyr
ENST00000342175.11:c.79466C>A (TTN)	ENSP00000340554.6:p.Ser26489Tyr
ENST00000359218.10:c.79265C>A (TTN)	ENSP00000352154.5:p.Ser26422Tyr
ENST00000342175.10:c.79466C>A (TTN)	ENSP00000340554.6:p.Ser26489Tyr
ENST00000342992.10:c.98381C>A (TTN)	ENSP00000343764.6:p.Ser32794Tyr
ENST00000359218.9:c.79265C>A (TTN)	ENSP00000352154.5:p.Ser26422Tyr
ENST00000460472.6:c.78890C>A (TTN)	ENSP00000434586.1:p.Ser26297Tyr
ENST00000589042.5:c.106085C>A (TTN) MANE Select	ENSP00000467141.1:p.Ser35362Tyr
ENST00000591111.5:c.101162C>A (TTN)	ENSP00000465570.1:p.Ser33721Tyr
ENST00000615779.4:c.101162C>A (TTN)	ENSP00000483597.1:p.Ser33721Tyr
NM_001256850.1:c.101162C>A (TTN)	NP_001243779.1:p.Ser33721Tyr
NM_001267550.2:c.106085C>A (TTN) MANE Select	NP_001254479.2:p.Ser35362Tyr
NM_003319.4:c.78890C>A (TTN)	NP_003310.4:p.Ser26297Tyr
NM_133378.4:c.98381C>A (TTN)	NP_596869.4:p.Ser32794Tyr
NM_133432.3:c.79265C>A (TTN)	NP_597676.3:p.Ser26422Tyr
NM_133437.4:c.79466C>A (TTN)	NP_597681.4:p.Ser26489Tyr
NR_038271.1:n.446+6894G>T (TTN-AS1)
NR_038272.1:n.220-5202G>T (TTN-AS1)
XM_011511729.1:c.105182C>A (TTN)	XP_011510031.1:p.Ser35061Tyr
XM_011511730.1:c.79076C>A (TTN)	XP_011510032.1:p.Ser26359Tyr
XM_011511731.1:c.78935C>A (TTN)	XP_011510033.1:p.Ser26312Tyr
XM_017004819.1:c.104978C>A (TTN)	XP_016860308.1:p.Ser34993Tyr
XM_017004820.1:c.100376C>A (TTN)	XP_016860309.1:p.Ser33459Tyr
XM_017004821.1:c.100373C>A (TTN)	XP_016860310.1:p.Ser33458Tyr
XM_017004822.1:c.97415C>A (TTN)	XP_016860311.1:p.Ser32472Tyr
XM_017004823.1:c.79031C>A (TTN)	XP_016860312.1:p.Ser26344Tyr
XM_024453094.1:c.100526C>A (TTN)	XP_024308862.1:p.Ser33509Tyr
XM_024453095.1:c.100523C>A (TTN)	XP_024308863.1:p.Ser33508Tyr
XM_024453096.1:c.99956C>A (TTN)	XP_024308864.1:p.Ser33319Tyr
XM_024453097.1:c.97298C>A (TTN)	XP_024308865.1:p.Ser32433Tyr
XM_024453098.1:c.97217C>A (TTN)	XP_024308866.1:p.Ser32406Tyr
XM_024453099.1:c.78980C>A (TTN)	XP_024308867.1:p.Ser26327Tyr
XM_024453100.1:c.68834C>A (TTN)	XP_024308868.1:p.Ser22945Tyr