Canonical Allele Identifier: CA349427114

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179401898T>G (hg19) ; chr2:g.178537171T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537171T>G , CM000664.2:g.178537171T>G	GRCh38
NC_000002.11:g.179401898T>G , CM000664.1:g.179401898T>G	GRCh37
NC_000002.10:g.179110144T>G	NCBI36
NG_011618.3:g.298632A>C , LRG_391:g.298632A>C
NG_051363.1:g.19345T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.92234A>C (TTN)	ENSP00000343764.6:p.Lys30745Thr
ENST00000342175.11:c.73319A>C (TTN)	ENSP00000340554.6:p.Lys24440Thr
ENST00000359218.10:c.73118A>C (TTN)	ENSP00000352154.5:p.Lys24373Thr
ENST00000342175.10:c.73319A>C (TTN)	ENSP00000340554.6:p.Lys24440Thr
ENST00000342992.10:c.92234A>C (TTN)	ENSP00000343764.6:p.Lys30745Thr
ENST00000359218.9:c.73118A>C (TTN)	ENSP00000352154.5:p.Lys24373Thr
ENST00000460472.6:c.72743A>C (TTN)	ENSP00000434586.1:p.Lys24248Thr
ENST00000589042.5:c.99938A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys33313Thr
ENST00000591111.5:c.95015A>C (TTN)	ENSP00000465570.1:p.Lys31672Thr
ENST00000615779.4:c.95015A>C (TTN)	ENSP00000483597.1:p.Lys31672Thr
NM_001256850.1:c.95015A>C (TTN)	NP_001243779.1:p.Lys31672Thr
NM_001267550.2:c.99938A>C (TTN) MANE Select	NP_001254479.2:p.Lys33313Thr
NM_003319.4:c.72743A>C (TTN)	NP_003310.4:p.Lys24248Thr
NM_133378.4:c.92234A>C (TTN)	NP_596869.4:p.Lys30745Thr
NM_133432.3:c.73118A>C (TTN)	NP_597676.3:p.Lys24373Thr
NM_133437.4:c.73319A>C (TTN)	NP_597681.4:p.Lys24440Thr
NR_038271.1:n.446+13535T>G (TTN-AS1)
NR_038272.1:n.317-190T>G (TTN-AS1)
XM_011511729.1:c.99035A>C (TTN)	XP_011510031.1:p.Lys33012Thr
XM_011511730.1:c.72929A>C (TTN)	XP_011510032.1:p.Lys24310Thr
XM_011511731.1:c.72788A>C (TTN)	XP_011510033.1:p.Lys24263Thr
XM_017004819.1:c.98831A>C (TTN)	XP_016860308.1:p.Lys32944Thr
XM_017004820.1:c.94229A>C (TTN)	XP_016860309.1:p.Lys31410Thr
XM_017004821.1:c.94226A>C (TTN)	XP_016860310.1:p.Lys31409Thr
XM_017004822.1:c.91268A>C (TTN)	XP_016860311.1:p.Lys30423Thr
XM_017004823.1:c.72884A>C (TTN)	XP_016860312.1:p.Lys24295Thr
XM_024453094.1:c.94379A>C (TTN)	XP_024308862.1:p.Lys31460Thr
XM_024453095.1:c.94376A>C (TTN)	XP_024308863.1:p.Lys31459Thr
XM_024453096.1:c.93809A>C (TTN)	XP_024308864.1:p.Lys31270Thr
XM_024453097.1:c.91151A>C (TTN)	XP_024308865.1:p.Lys30384Thr
XM_024453098.1:c.91070A>C (TTN)	XP_024308866.1:p.Lys30357Thr
XM_024453099.1:c.72833A>C (TTN)	XP_024308867.1:p.Lys24278Thr
XM_024453100.1:c.62687A>C (TTN)	XP_024308868.1:p.Lys20896Thr