Canonical Allele Identifier: CA349457340

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409147C>G (hg19) ; chr2:g.178544420C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544420C>G , CM000664.2:g.178544420C>G	GRCh38
NC_000002.11:g.179409147C>G , CM000664.1:g.179409147C>G	GRCh37
NC_000002.10:g.179117393C>G	NCBI36
NG_011618.3:g.291383G>C , LRG_391:g.291383G>C
NG_051363.1:g.26594C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88105G>C (TTN)	ENSP00000343764.6:p.Gly29369Arg
ENST00000342175.11:c.69190G>C (TTN)	ENSP00000340554.6:p.Gly23064Arg
ENST00000359218.10:c.68989G>C (TTN)	ENSP00000352154.5:p.Gly22997Arg
ENST00000342175.10:c.69190G>C (TTN)	ENSP00000340554.6:p.Gly23064Arg
ENST00000342992.10:c.88105G>C (TTN)	ENSP00000343764.6:p.Gly29369Arg
ENST00000359218.9:c.68989G>C (TTN)	ENSP00000352154.5:p.Gly22997Arg
ENST00000460472.6:c.68614G>C (TTN)	ENSP00000434586.1:p.Gly22872Arg
ENST00000589042.5:c.95809G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly31937Arg
ENST00000591111.5:c.90886G>C (TTN)	ENSP00000465570.1:p.Gly30296Arg
ENST00000615779.4:c.90886G>C (TTN)	ENSP00000483597.1:p.Gly30296Arg
NM_001256850.1:c.90886G>C (TTN)	NP_001243779.1:p.Gly30296Arg
NM_001267550.2:c.95809G>C (TTN) MANE Select	NP_001254479.2:p.Gly31937Arg
NM_003319.4:c.68614G>C (TTN)	NP_003310.4:p.Gly22872Arg
NM_133378.4:c.88105G>C (TTN)	NP_596869.4:p.Gly29369Arg
NM_133432.3:c.68989G>C (TTN)	NP_597676.3:p.Gly22997Arg
NM_133437.4:c.69190G>C (TTN)	NP_597681.4:p.Gly23064Arg
NR_038271.1:n.446+20784C>G (TTN-AS1)
NR_038272.1:n.2043+2059C>G (TTN-AS1)
XM_011511729.1:c.94906G>C (TTN)	XP_011510031.1:p.Gly31636Arg
XM_011511730.1:c.68800G>C (TTN)	XP_011510032.1:p.Gly22934Arg
XM_011511731.1:c.68659G>C (TTN)	XP_011510033.1:p.Gly22887Arg
XM_017004819.1:c.94702G>C (TTN)	XP_016860308.1:p.Gly31568Arg
XM_017004820.1:c.90100G>C (TTN)	XP_016860309.1:p.Gly30034Arg
XM_017004821.1:c.90097G>C (TTN)	XP_016860310.1:p.Gly30033Arg
XM_017004822.1:c.87139G>C (TTN)	XP_016860311.1:p.Gly29047Arg
XM_017004823.1:c.68755G>C (TTN)	XP_016860312.1:p.Gly22919Arg
XM_024453094.1:c.90250G>C (TTN)	XP_024308862.1:p.Gly30084Arg
XM_024453095.1:c.90247G>C (TTN)	XP_024308863.1:p.Gly30083Arg
XM_024453096.1:c.89680G>C (TTN)	XP_024308864.1:p.Gly29894Arg
XM_024453097.1:c.87022G>C (TTN)	XP_024308865.1:p.Gly29008Arg
XM_024453098.1:c.86941G>C (TTN)	XP_024308866.1:p.Gly28981Arg
XM_024453099.1:c.68704G>C (TTN)	XP_024308867.1:p.Gly22902Arg
XM_024453100.1:c.58558G>C (TTN)	XP_024308868.1:p.Gly19520Arg