Canonical Allele Identifier: CA349458205

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409207T>A (hg19) ; chr2:g.178544480T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544480T>A , CM000664.2:g.178544480T>A	GRCh38
NC_000002.11:g.179409207T>A , CM000664.1:g.179409207T>A	GRCh37
NC_000002.10:g.179117453T>A	NCBI36
NG_011618.3:g.291323A>T , LRG_391:g.291323A>T
NG_051363.1:g.26654T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88045A>T (TTN)	ENSP00000343764.6:p.Arg29349Ter
ENST00000342175.11:c.69130A>T (TTN)	ENSP00000340554.6:p.Arg23044Ter
ENST00000359218.10:c.68929A>T (TTN)	ENSP00000352154.5:p.Arg22977Ter
ENST00000342175.10:c.69130A>T (TTN)	ENSP00000340554.6:p.Arg23044Ter
ENST00000342992.10:c.88045A>T (TTN)	ENSP00000343764.6:p.Arg29349Ter
ENST00000359218.9:c.68929A>T (TTN)	ENSP00000352154.5:p.Arg22977Ter
ENST00000460472.6:c.68554A>T (TTN)	ENSP00000434586.1:p.Arg22852Ter
ENST00000589042.5:c.95749A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg31917Ter
ENST00000591111.5:c.90826A>T (TTN)	ENSP00000465570.1:p.Arg30276Ter
ENST00000615779.4:c.90826A>T (TTN)	ENSP00000483597.1:p.Arg30276Ter
NM_001256850.1:c.90826A>T (TTN)	NP_001243779.1:p.Arg30276Ter
NM_001267550.2:c.95749A>T (TTN) MANE Select	NP_001254479.2:p.Arg31917Ter
NM_003319.4:c.68554A>T (TTN)	NP_003310.4:p.Arg22852Ter
NM_133378.4:c.88045A>T (TTN)	NP_596869.4:p.Arg29349Ter
NM_133432.3:c.68929A>T (TTN)	NP_597676.3:p.Arg22977Ter
NM_133437.4:c.69130A>T (TTN)	NP_597681.4:p.Arg23044Ter
NR_038271.1:n.446+20844T>A (TTN-AS1)
NR_038272.1:n.2043+2119T>A (TTN-AS1)
XM_011511729.1:c.94846A>T (TTN)	XP_011510031.1:p.Arg31616Ter
XM_011511730.1:c.68740A>T (TTN)	XP_011510032.1:p.Arg22914Ter
XM_011511731.1:c.68599A>T (TTN)	XP_011510033.1:p.Arg22867Ter
XM_017004819.1:c.94642A>T (TTN)	XP_016860308.1:p.Arg31548Ter
XM_017004820.1:c.90040A>T (TTN)	XP_016860309.1:p.Arg30014Ter
XM_017004821.1:c.90037A>T (TTN)	XP_016860310.1:p.Arg30013Ter
XM_017004822.1:c.87079A>T (TTN)	XP_016860311.1:p.Arg29027Ter
XM_017004823.1:c.68695A>T (TTN)	XP_016860312.1:p.Arg22899Ter
XM_024453094.1:c.90190A>T (TTN)	XP_024308862.1:p.Arg30064Ter
XM_024453095.1:c.90187A>T (TTN)	XP_024308863.1:p.Arg30063Ter
XM_024453096.1:c.89620A>T (TTN)	XP_024308864.1:p.Arg29874Ter
XM_024453097.1:c.86962A>T (TTN)	XP_024308865.1:p.Arg28988Ter
XM_024453098.1:c.86881A>T (TTN)	XP_024308866.1:p.Arg28961Ter
XM_024453099.1:c.68644A>T (TTN)	XP_024308867.1:p.Arg22882Ter
XM_024453100.1:c.58498A>T (TTN)	XP_024308868.1:p.Arg19500Ter