Canonical Allele Identifier: CA349456184

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409057T>A (hg19) ; chr2:g.178544330T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544330T>A , CM000664.2:g.178544330T>A	GRCh38
NC_000002.11:g.179409057T>A , CM000664.1:g.179409057T>A	GRCh37
NC_000002.10:g.179117303T>A	NCBI36
NG_011618.3:g.291473A>T , LRG_391:g.291473A>T
NG_051363.1:g.26504T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88195A>T (TTN)	ENSP00000343764.6:p.Asn29399Tyr
ENST00000342175.11:c.69280A>T (TTN)	ENSP00000340554.6:p.Asn23094Tyr
ENST00000359218.10:c.69079A>T (TTN)	ENSP00000352154.5:p.Asn23027Tyr
ENST00000342175.10:c.69280A>T (TTN)	ENSP00000340554.6:p.Asn23094Tyr
ENST00000342992.10:c.88195A>T (TTN)	ENSP00000343764.6:p.Asn29399Tyr
ENST00000359218.9:c.69079A>T (TTN)	ENSP00000352154.5:p.Asn23027Tyr
ENST00000460472.6:c.68704A>T (TTN)	ENSP00000434586.1:p.Asn22902Tyr
ENST00000589042.5:c.95899A>T (TTN) MANE Select	ENSP00000467141.1:p.Asn31967Tyr
ENST00000591111.5:c.90976A>T (TTN)	ENSP00000465570.1:p.Asn30326Tyr
ENST00000615779.4:c.90976A>T (TTN)	ENSP00000483597.1:p.Asn30326Tyr
NM_001256850.1:c.90976A>T (TTN)	NP_001243779.1:p.Asn30326Tyr
NM_001267550.2:c.95899A>T (TTN) MANE Select	NP_001254479.2:p.Asn31967Tyr
NM_003319.4:c.68704A>T (TTN)	NP_003310.4:p.Asn22902Tyr
NM_133378.4:c.88195A>T (TTN)	NP_596869.4:p.Asn29399Tyr
NM_133432.3:c.69079A>T (TTN)	NP_597676.3:p.Asn23027Tyr
NM_133437.4:c.69280A>T (TTN)	NP_597681.4:p.Asn23094Tyr
NR_038271.1:n.446+20694T>A (TTN-AS1)
NR_038272.1:n.2043+1969T>A (TTN-AS1)
XM_011511729.1:c.94996A>T (TTN)	XP_011510031.1:p.Asn31666Tyr
XM_011511730.1:c.68890A>T (TTN)	XP_011510032.1:p.Asn22964Tyr
XM_011511731.1:c.68749A>T (TTN)	XP_011510033.1:p.Asn22917Tyr
XM_017004819.1:c.94792A>T (TTN)	XP_016860308.1:p.Asn31598Tyr
XM_017004820.1:c.90190A>T (TTN)	XP_016860309.1:p.Asn30064Tyr
XM_017004821.1:c.90187A>T (TTN)	XP_016860310.1:p.Asn30063Tyr
XM_017004822.1:c.87229A>T (TTN)	XP_016860311.1:p.Asn29077Tyr
XM_017004823.1:c.68845A>T (TTN)	XP_016860312.1:p.Asn22949Tyr
XM_024453094.1:c.90340A>T (TTN)	XP_024308862.1:p.Asn30114Tyr
XM_024453095.1:c.90337A>T (TTN)	XP_024308863.1:p.Asn30113Tyr
XM_024453096.1:c.89770A>T (TTN)	XP_024308864.1:p.Asn29924Tyr
XM_024453097.1:c.87112A>T (TTN)	XP_024308865.1:p.Asn29038Tyr
XM_024453098.1:c.87031A>T (TTN)	XP_024308866.1:p.Asn29011Tyr
XM_024453099.1:c.68794A>T (TTN)	XP_024308867.1:p.Asn22932Tyr
XM_024453100.1:c.58648A>T (TTN)	XP_024308868.1:p.Asn19550Tyr