Canonical Allele Identifier: CA2740096117

Gene: TTN TTN-AS1

Linked Data

• ClinVar Variation Id: 2945821
• ClinVar RCV Id: RCV003803915

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607772T>C , CM000664.2:g.178607772T>C	GRCh38
NC_000002.11:g.179472499T>C , CM000664.1:g.179472499T>C	GRCh37
NC_000002.10:g.179180744T>C	NCBI36
NG_011618.3:g.228031A>G , LRG_391:g.228031A>G
NG_051363.1:g.89946T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45298+13A>G (TTN)	ENSP00000343764.6:n.45298+13A>G
ENST00000342175.11:c.26383+13A>G (TTN)	ENSP00000340554.6:n.26383+13A>G
ENST00000359218.10:c.26182+13A>G (TTN)	ENSP00000352154.5:n.26182+13A>G
ENST00000342175.10:c.26383+13A>G (TTN)	ENSP00000340554.6:n.26383+13A>G
ENST00000342992.10:c.45298+13A>G (TTN)	ENSP00000343764.6:n.45298+13A>G
ENST00000359218.9:c.26182+13A>G (TTN)	ENSP00000352154.5:n.26182+13A>G
ENST00000460472.6:c.25807+13A>G (TTN)	ENSP00000434586.1:n.25807+13A>G
ENST00000589042.5:c.53002+13A>G (TTN) MANE Select	ENSP00000467141.1:n.53002+13A>G
ENST00000591111.5:c.48079+13A>G (TTN)	ENSP00000465570.1:n.48079+13A>G
ENST00000615779.4:c.48079+13A>G (TTN)	ENSP00000483597.1:n.48079+13A>G
NM_001256850.1:c.48079+13A>G (TTN)	NP_001243779.1:n.48079+13A>G
NM_001267550.2:c.53002+13A>G (TTN) MANE Select	NP_001254479.2:n.53002+13A>G
NM_003319.4:c.25807+13A>G (TTN)	NP_003310.4:n.25807+13A>G
NM_133378.4:c.45298+13A>G (TTN)	NP_596869.4:n.45298+13A>G
NM_133432.3:c.26182+13A>G (TTN)	NP_597676.3:n.26182+13A>G
NM_133437.4:c.26383+13A>G (TTN)	NP_597681.4:n.26383+13A>G
NR_038271.1:n.683-395T>C (TTN-AS1)
XM_011511729.1:c.52099+13A>G (TTN)	XP_011510031.1:n.52099+13A>G
XM_011511730.1:c.25993+13A>G (TTN)	XP_011510032.1:n.25993+13A>G
XM_011511731.1:c.25852+13A>G (TTN)	XP_011510033.1:n.25852+13A>G
XM_017004819.1:c.51895+13A>G (TTN)	XP_016860308.1:n.51895+13A>G
XM_017004820.1:c.47293+13A>G (TTN)	XP_016860309.1:n.47293+13A>G
XM_017004821.1:c.47290+13A>G (TTN)	XP_016860310.1:n.47290+13A>G
XM_017004822.1:c.44332+13A>G (TTN)	XP_016860311.1:n.44332+13A>G
XM_017004823.1:c.25948+13A>G (TTN)	XP_016860312.1:n.25948+13A>G
XM_024453094.1:c.47443+13A>G (TTN)	XP_024308862.1:n.47443+13A>G
XM_024453095.1:c.47440+13A>G (TTN)	XP_024308863.1:n.47440+13A>G
XM_024453096.1:c.46873+13A>G (TTN)	XP_024308864.1:n.46873+13A>G
XM_024453097.1:c.44215+13A>G (TTN)	XP_024308865.1:n.44215+13A>G
XM_024453098.1:c.44134+13A>G (TTN)	XP_024308866.1:n.44134+13A>G
XM_024453099.1:c.25897+13A>G (TTN)	XP_024308867.1:n.25897+13A>G
XM_024453100.1:c.15751+13A>G (TTN)	XP_024308868.1:n.15751+13A>G