Canonical Allele Identifier: CA349457339

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88105G>A (TTN)	ENSP00000343764.6:p.Gly29369Ser
ENST00000342175.11:c.69190G>A (TTN)	ENSP00000340554.6:p.Gly23064Ser
ENST00000359218.10:c.68989G>A (TTN)	ENSP00000352154.5:p.Gly22997Ser
ENST00000342175.10:c.69190G>A (TTN)	ENSP00000340554.6:p.Gly23064Ser
ENST00000342992.10:c.88105G>A (TTN)	ENSP00000343764.6:p.Gly29369Ser
ENST00000359218.9:c.68989G>A (TTN)	ENSP00000352154.5:p.Gly22997Ser
ENST00000460472.6:c.68614G>A (TTN)	ENSP00000434586.1:p.Gly22872Ser
ENST00000589042.5:c.95809G>A (TTN) MANE Select	ENSP00000467141.1:p.Gly31937Ser
ENST00000591111.5:c.90886G>A (TTN)	ENSP00000465570.1:p.Gly30296Ser
ENST00000615779.4:c.90886G>A (TTN)	ENSP00000483597.1:p.Gly30296Ser
NM_001256850.1:c.90886G>A (TTN)	NP_001243779.1:p.Gly30296Ser
NM_001267550.2:c.95809G>A (TTN) MANE Select	NP_001254479.2:p.Gly31937Ser
NM_003319.4:c.68614G>A (TTN)	NP_003310.4:p.Gly22872Ser
NM_133378.4:c.88105G>A (TTN)	NP_596869.4:p.Gly29369Ser
NM_133432.3:c.68989G>A (TTN)	NP_597676.3:p.Gly22997Ser
NM_133437.4:c.69190G>A (TTN)	NP_597681.4:p.Gly23064Ser
NR_038271.1:n.446+20784C>T (TTN-AS1)
NR_038272.1:n.2043+2059C>T (TTN-AS1)
XM_011511729.1:c.94906G>A (TTN)	XP_011510031.1:p.Gly31636Ser
XM_011511730.1:c.68800G>A (TTN)	XP_011510032.1:p.Gly22934Ser
XM_011511731.1:c.68659G>A (TTN)	XP_011510033.1:p.Gly22887Ser
XM_017004819.1:c.94702G>A (TTN)	XP_016860308.1:p.Gly31568Ser
XM_017004820.1:c.90100G>A (TTN)	XP_016860309.1:p.Gly30034Ser
XM_017004821.1:c.90097G>A (TTN)	XP_016860310.1:p.Gly30033Ser
XM_017004822.1:c.87139G>A (TTN)	XP_016860311.1:p.Gly29047Ser
XM_017004823.1:c.68755G>A (TTN)	XP_016860312.1:p.Gly22919Ser
XM_024453094.1:c.90250G>A (TTN)	XP_024308862.1:p.Gly30084Ser
XM_024453095.1:c.90247G>A (TTN)	XP_024308863.1:p.Gly30083Ser
XM_024453096.1:c.89680G>A (TTN)	XP_024308864.1:p.Gly29894Ser
XM_024453097.1:c.87022G>A (TTN)	XP_024308865.1:p.Gly29008Ser
XM_024453098.1:c.86941G>A (TTN)	XP_024308866.1:p.Gly28981Ser
XM_024453099.1:c.68704G>A (TTN)	XP_024308867.1:p.Gly22902Ser
XM_024453100.1:c.58558G>A (TTN)	XP_024308868.1:p.Gly19520Ser