Canonical Allele Identifier: CA430241704

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408661T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543934T>C , CM000664.2:g.178543934T>C	GRCh38
NC_000002.11:g.179408661T>C , CM000664.1:g.179408661T>C	GRCh37
NC_000002.10:g.179116907T>C	NCBI36
NG_011618.3:g.291869A>G , LRG_391:g.291869A>G
NG_051363.1:g.26108T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88506A>G (TTN)	ENSP00000343764.6:p.Leu29502=
ENST00000342175.11:c.69591A>G (TTN)	ENSP00000340554.6:p.Leu23197=
ENST00000359218.10:c.69390A>G (TTN)	ENSP00000352154.5:p.Leu23130=
ENST00000342175.10:c.69591A>G (TTN)	ENSP00000340554.6:p.Leu23197=
ENST00000342992.10:c.88506A>G (TTN)	ENSP00000343764.6:p.Leu29502=
ENST00000359218.9:c.69390A>G (TTN)	ENSP00000352154.5:p.Leu23130=
ENST00000460472.6:c.69015A>G (TTN)	ENSP00000434586.1:p.Leu23005=
ENST00000589042.5:c.96210A>G (TTN) MANE Select	ENSP00000467141.1:p.Leu32070=
ENST00000591111.5:c.91287A>G (TTN)	ENSP00000465570.1:p.Leu30429=
ENST00000615779.4:c.91287A>G (TTN)	ENSP00000483597.1:p.Leu30429=
NM_001256850.1:c.91287A>G (TTN)	NP_001243779.1:p.Leu30429=
NM_001267550.2:c.96210A>G (TTN) MANE Select	NP_001254479.2:p.Leu32070=
NM_003319.4:c.69015A>G (TTN)	NP_003310.4:p.Leu23005=
NM_133378.4:c.88506A>G (TTN)	NP_596869.4:p.Leu29502=
NM_133432.3:c.69390A>G (TTN)	NP_597676.3:p.Leu23130=
NM_133437.4:c.69591A>G (TTN)	NP_597681.4:p.Leu23197=
NR_038271.1:n.446+20298T>C (TTN-AS1)
NR_038272.1:n.2043+1573T>C (TTN-AS1)
XM_011511729.1:c.95307A>G (TTN)	XP_011510031.1:p.Leu31769=
XM_011511730.1:c.69201A>G (TTN)	XP_011510032.1:p.Leu23067=
XM_011511731.1:c.69060A>G (TTN)	XP_011510033.1:p.Leu23020=
XM_017004819.1:c.95103A>G (TTN)	XP_016860308.1:p.Leu31701=
XM_017004820.1:c.90501A>G (TTN)	XP_016860309.1:p.Leu30167=
XM_017004821.1:c.90498A>G (TTN)	XP_016860310.1:p.Leu30166=
XM_017004822.1:c.87540A>G (TTN)	XP_016860311.1:p.Leu29180=
XM_017004823.1:c.69156A>G (TTN)	XP_016860312.1:p.Leu23052=
XM_024453094.1:c.90651A>G (TTN)	XP_024308862.1:p.Leu30217=
XM_024453095.1:c.90648A>G (TTN)	XP_024308863.1:p.Leu30216=
XM_024453096.1:c.90081A>G (TTN)	XP_024308864.1:p.Leu30027=
XM_024453097.1:c.87423A>G (TTN)	XP_024308865.1:p.Leu29141=
XM_024453098.1:c.87342A>G (TTN)	XP_024308866.1:p.Leu29114=
XM_024453099.1:c.69105A>G (TTN)	XP_024308867.1:p.Leu23035=
XM_024453100.1:c.58959A>G (TTN)	XP_024308868.1:p.Leu19653=