Canonical Allele Identifier: CA349427115

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.92234A>G (TTN)	ENSP00000343764.6:p.Lys30745Arg
ENST00000342175.11:c.73319A>G (TTN)	ENSP00000340554.6:p.Lys24440Arg
ENST00000359218.10:c.73118A>G (TTN)	ENSP00000352154.5:p.Lys24373Arg
ENST00000342175.10:c.73319A>G (TTN)	ENSP00000340554.6:p.Lys24440Arg
ENST00000342992.10:c.92234A>G (TTN)	ENSP00000343764.6:p.Lys30745Arg
ENST00000359218.9:c.73118A>G (TTN)	ENSP00000352154.5:p.Lys24373Arg
ENST00000460472.6:c.72743A>G (TTN)	ENSP00000434586.1:p.Lys24248Arg
ENST00000589042.5:c.99938A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys33313Arg
ENST00000591111.5:c.95015A>G (TTN)	ENSP00000465570.1:p.Lys31672Arg
ENST00000615779.4:c.95015A>G (TTN)	ENSP00000483597.1:p.Lys31672Arg
NM_001256850.1:c.95015A>G (TTN)	NP_001243779.1:p.Lys31672Arg
NM_001267550.2:c.99938A>G (TTN) MANE Select	NP_001254479.2:p.Lys33313Arg
NM_003319.4:c.72743A>G (TTN)	NP_003310.4:p.Lys24248Arg
NM_133378.4:c.92234A>G (TTN)	NP_596869.4:p.Lys30745Arg
NM_133432.3:c.73118A>G (TTN)	NP_597676.3:p.Lys24373Arg
NM_133437.4:c.73319A>G (TTN)	NP_597681.4:p.Lys24440Arg
NR_038271.1:n.446+13535T>C (TTN-AS1)
NR_038272.1:n.317-190T>C (TTN-AS1)
XM_011511729.1:c.99035A>G (TTN)	XP_011510031.1:p.Lys33012Arg
XM_011511730.1:c.72929A>G (TTN)	XP_011510032.1:p.Lys24310Arg
XM_011511731.1:c.72788A>G (TTN)	XP_011510033.1:p.Lys24263Arg
XM_017004819.1:c.98831A>G (TTN)	XP_016860308.1:p.Lys32944Arg
XM_017004820.1:c.94229A>G (TTN)	XP_016860309.1:p.Lys31410Arg
XM_017004821.1:c.94226A>G (TTN)	XP_016860310.1:p.Lys31409Arg
XM_017004822.1:c.91268A>G (TTN)	XP_016860311.1:p.Lys30423Arg
XM_017004823.1:c.72884A>G (TTN)	XP_016860312.1:p.Lys24295Arg
XM_024453094.1:c.94379A>G (TTN)	XP_024308862.1:p.Lys31460Arg
XM_024453095.1:c.94376A>G (TTN)	XP_024308863.1:p.Lys31459Arg
XM_024453096.1:c.93809A>G (TTN)	XP_024308864.1:p.Lys31270Arg
XM_024453097.1:c.91151A>G (TTN)	XP_024308865.1:p.Lys30384Arg
XM_024453098.1:c.91070A>G (TTN)	XP_024308866.1:p.Lys30357Arg
XM_024453099.1:c.72833A>G (TTN)	XP_024308867.1:p.Lys24278Arg
XM_024453100.1:c.62687A>G (TTN)	XP_024308868.1:p.Lys20896Arg