Canonical Allele Identifier: CA2580064955

Gene: TTN TTN-AS1

Linked Data

• ClinVar Variation Id: 2036725
• ClinVar RCV Id: RCV002882027

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577978A>G , CM000664.2:g.178577978A>G	GRCh38
NC_000002.11:g.179442705A>G , CM000664.1:g.179442705A>G	GRCh37
NC_000002.10:g.179150951A>G	NCBI36
NG_011618.3:g.257825T>C , LRG_391:g.257825T>C
NG_051363.1:g.60152A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.60823+10T>C (TTN)	ENSP00000343764.6:n.60823+10T>C
ENST00000342175.11:c.41908+10T>C (TTN)	ENSP00000340554.6:n.41908+10T>C
ENST00000359218.10:c.41707+10T>C (TTN)	ENSP00000352154.5:n.41707+10T>C
ENST00000342175.10:c.41908+10T>C (TTN)	ENSP00000340554.6:n.41908+10T>C
ENST00000342992.10:c.60823+10T>C (TTN)	ENSP00000343764.6:n.60823+10T>C
ENST00000359218.9:c.41707+10T>C (TTN)	ENSP00000352154.5:n.41707+10T>C
ENST00000460472.6:c.41332+10T>C (TTN)	ENSP00000434586.1:n.41332+10T>C
ENST00000589042.5:c.68527+10T>C (TTN) MANE Select	ENSP00000467141.1:n.68527+10T>C
ENST00000591111.5:c.63604+10T>C (TTN)	ENSP00000465570.1:n.63604+10T>C
ENST00000615779.4:c.63604+10T>C (TTN)	ENSP00000483597.1:n.63604+10T>C
NM_001256850.1:c.63604+10T>C (TTN)	NP_001243779.1:n.63604+10T>C
NM_001267550.2:c.68527+10T>C (TTN) MANE Select	NP_001254479.2:n.68527+10T>C
NM_003319.4:c.41332+10T>C (TTN)	NP_003310.4:n.41332+10T>C
NM_133378.4:c.60823+10T>C (TTN)	NP_596869.4:n.60823+10T>C
NM_133432.3:c.41707+10T>C (TTN)	NP_597676.3:n.41707+10T>C
NM_133437.4:c.41908+10T>C (TTN)	NP_597681.4:n.41908+10T>C
NR_038271.1:n.596+6529A>G (TTN-AS1)
NR_038272.1:n.2044-4594A>G (TTN-AS1)
XM_011511729.1:c.67624+10T>C (TTN)	XP_011510031.1:n.67624+10T>C
XM_011511730.1:c.41518+10T>C (TTN)	XP_011510032.1:n.41518+10T>C
XM_011511731.1:c.41377+10T>C (TTN)	XP_011510033.1:n.41377+10T>C
XM_017004819.1:c.67420+10T>C (TTN)	XP_016860308.1:n.67420+10T>C
XM_017004820.1:c.62818+10T>C (TTN)	XP_016860309.1:n.62818+10T>C
XM_017004821.1:c.62815+10T>C (TTN)	XP_016860310.1:n.62815+10T>C
XM_017004822.1:c.59857+10T>C (TTN)	XP_016860311.1:n.59857+10T>C
XM_017004823.1:c.41473+10T>C (TTN)	XP_016860312.1:n.41473+10T>C
XM_024453094.1:c.62968+10T>C (TTN)	XP_024308862.1:n.62968+10T>C
XM_024453095.1:c.62965+10T>C (TTN)	XP_024308863.1:n.62965+10T>C
XM_024453096.1:c.62398+10T>C (TTN)	XP_024308864.1:n.62398+10T>C
XM_024453097.1:c.59740+10T>C (TTN)	XP_024308865.1:n.59740+10T>C
XM_024453098.1:c.59659+10T>C (TTN)	XP_024308866.1:n.59659+10T>C
XM_024453099.1:c.41422+10T>C (TTN)	XP_024308867.1:n.41422+10T>C
XM_024453100.1:c.31276+10T>C (TTN)	XP_024308868.1:n.31276+10T>C