Canonical Allele Identifier: CA349407160

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395300T>C (hg19) ; chr2:g.178530573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530573T>C , CM000664.2:g.178530573T>C	GRCh38
NC_000002.11:g.179395300T>C , CM000664.1:g.179395300T>C	GRCh37
NC_000002.10:g.179103546T>C	NCBI36
NG_011618.3:g.305230A>G , LRG_391:g.305230A>G
NG_051363.1:g.12747T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98338A>G (TTN)	ENSP00000343764.6:p.Asn32780Asp
ENST00000342175.11:c.79423A>G (TTN)	ENSP00000340554.6:p.Asn26475Asp
ENST00000359218.10:c.79222A>G (TTN)	ENSP00000352154.5:p.Asn26408Asp
ENST00000342175.10:c.79423A>G (TTN)	ENSP00000340554.6:p.Asn26475Asp
ENST00000342992.10:c.98338A>G (TTN)	ENSP00000343764.6:p.Asn32780Asp
ENST00000359218.9:c.79222A>G (TTN)	ENSP00000352154.5:p.Asn26408Asp
ENST00000460472.6:c.78847A>G (TTN)	ENSP00000434586.1:p.Asn26283Asp
ENST00000589042.5:c.106042A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn35348Asp
ENST00000591111.5:c.101119A>G (TTN)	ENSP00000465570.1:p.Asn33707Asp
ENST00000615779.4:c.101119A>G (TTN)	ENSP00000483597.1:p.Asn33707Asp
NM_001256850.1:c.101119A>G (TTN)	NP_001243779.1:p.Asn33707Asp
NM_001267550.2:c.106042A>G (TTN) MANE Select	NP_001254479.2:p.Asn35348Asp
NM_003319.4:c.78847A>G (TTN)	NP_003310.4:p.Asn26283Asp
NM_133378.4:c.98338A>G (TTN)	NP_596869.4:p.Asn32780Asp
NM_133432.3:c.79222A>G (TTN)	NP_597676.3:p.Asn26408Asp
NM_133437.4:c.79423A>G (TTN)	NP_597681.4:p.Asn26475Asp
NR_038271.1:n.446+6937T>C (TTN-AS1)
NR_038272.1:n.220-5159T>C (TTN-AS1)
XM_011511729.1:c.105139A>G (TTN)	XP_011510031.1:p.Asn35047Asp
XM_011511730.1:c.79033A>G (TTN)	XP_011510032.1:p.Asn26345Asp
XM_011511731.1:c.78892A>G (TTN)	XP_011510033.1:p.Asn26298Asp
XM_017004819.1:c.104935A>G (TTN)	XP_016860308.1:p.Asn34979Asp
XM_017004820.1:c.100333A>G (TTN)	XP_016860309.1:p.Asn33445Asp
XM_017004821.1:c.100330A>G (TTN)	XP_016860310.1:p.Asn33444Asp
XM_017004822.1:c.97372A>G (TTN)	XP_016860311.1:p.Asn32458Asp
XM_017004823.1:c.78988A>G (TTN)	XP_016860312.1:p.Asn26330Asp
XM_024453094.1:c.100483A>G (TTN)	XP_024308862.1:p.Asn33495Asp
XM_024453095.1:c.100480A>G (TTN)	XP_024308863.1:p.Asn33494Asp
XM_024453096.1:c.99913A>G (TTN)	XP_024308864.1:p.Asn33305Asp
XM_024453097.1:c.97255A>G (TTN)	XP_024308865.1:p.Asn32419Asp
XM_024453098.1:c.97174A>G (TTN)	XP_024308866.1:p.Asn32392Asp
XM_024453099.1:c.78937A>G (TTN)	XP_024308867.1:p.Asn26313Asp
XM_024453100.1:c.68791A>G (TTN)	XP_024308868.1:p.Asn22931Asp