Canonical Allele Identifier: CA349411609

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396862C>G (hg19) ; chr2:g.178532135C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532135C>G , CM000664.2:g.178532135C>G	GRCh38
NC_000002.11:g.179396862C>G , CM000664.1:g.179396862C>G	GRCh37
NC_000002.10:g.179105108C>G	NCBI36
NG_011618.3:g.303668G>C , LRG_391:g.303668G>C
NG_051363.1:g.14309C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96776G>C (TTN)	ENSP00000343764.6:p.Arg32259Thr
ENST00000342175.11:c.77861G>C (TTN)	ENSP00000340554.6:p.Arg25954Thr
ENST00000359218.10:c.77660G>C (TTN)	ENSP00000352154.5:p.Arg25887Thr
ENST00000342175.10:c.77861G>C (TTN)	ENSP00000340554.6:p.Arg25954Thr
ENST00000342992.10:c.96776G>C (TTN)	ENSP00000343764.6:p.Arg32259Thr
ENST00000359218.9:c.77660G>C (TTN)	ENSP00000352154.5:p.Arg25887Thr
ENST00000460472.6:c.77285G>C (TTN)	ENSP00000434586.1:p.Arg25762Thr
ENST00000589042.5:c.104480G>C (TTN) MANE Select	ENSP00000467141.1:p.Arg34827Thr
ENST00000591111.5:c.99557G>C (TTN)	ENSP00000465570.1:p.Arg33186Thr
ENST00000615779.4:c.99557G>C (TTN)	ENSP00000483597.1:p.Arg33186Thr
NM_001256850.1:c.99557G>C (TTN)	NP_001243779.1:p.Arg33186Thr
NM_001267550.2:c.104480G>C (TTN) MANE Select	NP_001254479.2:p.Arg34827Thr
NM_003319.4:c.77285G>C (TTN)	NP_003310.4:p.Arg25762Thr
NM_133378.4:c.96776G>C (TTN)	NP_596869.4:p.Arg32259Thr
NM_133432.3:c.77660G>C (TTN)	NP_597676.3:p.Arg25887Thr
NM_133437.4:c.77861G>C (TTN)	NP_597681.4:p.Arg25954Thr
NR_038271.1:n.446+8499C>G (TTN-AS1)
NR_038272.1:n.220-3597C>G (TTN-AS1)
XM_011511729.1:c.103577G>C (TTN)	XP_011510031.1:p.Arg34526Thr
XM_011511730.1:c.77471G>C (TTN)	XP_011510032.1:p.Arg25824Thr
XM_011511731.1:c.77330G>C (TTN)	XP_011510033.1:p.Arg25777Thr
XM_017004819.1:c.103373G>C (TTN)	XP_016860308.1:p.Arg34458Thr
XM_017004820.1:c.98771G>C (TTN)	XP_016860309.1:p.Arg32924Thr
XM_017004821.1:c.98768G>C (TTN)	XP_016860310.1:p.Arg32923Thr
XM_017004822.1:c.95810G>C (TTN)	XP_016860311.1:p.Arg31937Thr
XM_017004823.1:c.77426G>C (TTN)	XP_016860312.1:p.Arg25809Thr
XM_024453094.1:c.98921G>C (TTN)	XP_024308862.1:p.Arg32974Thr
XM_024453095.1:c.98918G>C (TTN)	XP_024308863.1:p.Arg32973Thr
XM_024453096.1:c.98351G>C (TTN)	XP_024308864.1:p.Arg32784Thr
XM_024453097.1:c.95693G>C (TTN)	XP_024308865.1:p.Arg31898Thr
XM_024453098.1:c.95612G>C (TTN)	XP_024308866.1:p.Arg31871Thr
XM_024453099.1:c.77375G>C (TTN)	XP_024308867.1:p.Arg25792Thr
XM_024453100.1:c.67229G>C (TTN)	XP_024308868.1:p.Arg22410Thr