Canonical Allele Identifier: CA349457395

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409152T>C (hg19) ; chr2:g.178544425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544425T>C , CM000664.2:g.178544425T>C	GRCh38
NC_000002.11:g.179409152T>C , CM000664.1:g.179409152T>C	GRCh37
NC_000002.10:g.179117398T>C	NCBI36
NG_011618.3:g.291378A>G , LRG_391:g.291378A>G
NG_051363.1:g.26599T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88100A>G (TTN)	ENSP00000343764.6:p.Tyr29367Cys
ENST00000342175.11:c.69185A>G (TTN)	ENSP00000340554.6:p.Tyr23062Cys
ENST00000359218.10:c.68984A>G (TTN)	ENSP00000352154.5:p.Tyr22995Cys
ENST00000342175.10:c.69185A>G (TTN)	ENSP00000340554.6:p.Tyr23062Cys
ENST00000342992.10:c.88100A>G (TTN)	ENSP00000343764.6:p.Tyr29367Cys
ENST00000359218.9:c.68984A>G (TTN)	ENSP00000352154.5:p.Tyr22995Cys
ENST00000460472.6:c.68609A>G (TTN)	ENSP00000434586.1:p.Tyr22870Cys
ENST00000589042.5:c.95804A>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr31935Cys
ENST00000591111.5:c.90881A>G (TTN)	ENSP00000465570.1:p.Tyr30294Cys
ENST00000615779.4:c.90881A>G (TTN)	ENSP00000483597.1:p.Tyr30294Cys
NM_001256850.1:c.90881A>G (TTN)	NP_001243779.1:p.Tyr30294Cys
NM_001267550.2:c.95804A>G (TTN) MANE Select	NP_001254479.2:p.Tyr31935Cys
NM_003319.4:c.68609A>G (TTN)	NP_003310.4:p.Tyr22870Cys
NM_133378.4:c.88100A>G (TTN)	NP_596869.4:p.Tyr29367Cys
NM_133432.3:c.68984A>G (TTN)	NP_597676.3:p.Tyr22995Cys
NM_133437.4:c.69185A>G (TTN)	NP_597681.4:p.Tyr23062Cys
NR_038271.1:n.446+20789T>C (TTN-AS1)
NR_038272.1:n.2043+2064T>C (TTN-AS1)
XM_011511729.1:c.94901A>G (TTN)	XP_011510031.1:p.Tyr31634Cys
XM_011511730.1:c.68795A>G (TTN)	XP_011510032.1:p.Tyr22932Cys
XM_011511731.1:c.68654A>G (TTN)	XP_011510033.1:p.Tyr22885Cys
XM_017004819.1:c.94697A>G (TTN)	XP_016860308.1:p.Tyr31566Cys
XM_017004820.1:c.90095A>G (TTN)	XP_016860309.1:p.Tyr30032Cys
XM_017004821.1:c.90092A>G (TTN)	XP_016860310.1:p.Tyr30031Cys
XM_017004822.1:c.87134A>G (TTN)	XP_016860311.1:p.Tyr29045Cys
XM_017004823.1:c.68750A>G (TTN)	XP_016860312.1:p.Tyr22917Cys
XM_024453094.1:c.90245A>G (TTN)	XP_024308862.1:p.Tyr30082Cys
XM_024453095.1:c.90242A>G (TTN)	XP_024308863.1:p.Tyr30081Cys
XM_024453096.1:c.89675A>G (TTN)	XP_024308864.1:p.Tyr29892Cys
XM_024453097.1:c.87017A>G (TTN)	XP_024308865.1:p.Tyr29006Cys
XM_024453098.1:c.86936A>G (TTN)	XP_024308866.1:p.Tyr28979Cys
XM_024453099.1:c.68699A>G (TTN)	XP_024308867.1:p.Tyr22900Cys
XM_024453100.1:c.58553A>G (TTN)	XP_024308868.1:p.Tyr19518Cys