Canonical Allele Identifier: CA349406952

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395204T>C (hg19) ; chr2:g.178530477T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530477T>C , CM000664.2:g.178530477T>C	GRCh38
NC_000002.11:g.179395204T>C , CM000664.1:g.179395204T>C	GRCh37
NC_000002.10:g.179103450T>C	NCBI36
NG_011618.3:g.305326A>G , LRG_391:g.305326A>G
NG_051363.1:g.12651T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98434A>G (TTN)	ENSP00000343764.6:p.Lys32812Glu
ENST00000342175.11:c.79519A>G (TTN)	ENSP00000340554.6:p.Lys26507Glu
ENST00000359218.10:c.79318A>G (TTN)	ENSP00000352154.5:p.Lys26440Glu
ENST00000342175.10:c.79519A>G (TTN)	ENSP00000340554.6:p.Lys26507Glu
ENST00000342992.10:c.98434A>G (TTN)	ENSP00000343764.6:p.Lys32812Glu
ENST00000359218.9:c.79318A>G (TTN)	ENSP00000352154.5:p.Lys26440Glu
ENST00000460472.6:c.78943A>G (TTN)	ENSP00000434586.1:p.Lys26315Glu
ENST00000589042.5:c.106138A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35380Glu
ENST00000591111.5:c.101215A>G (TTN)	ENSP00000465570.1:p.Lys33739Glu
ENST00000615779.4:c.101215A>G (TTN)	ENSP00000483597.1:p.Lys33739Glu
NM_001256850.1:c.101215A>G (TTN)	NP_001243779.1:p.Lys33739Glu
NM_001267550.2:c.106138A>G (TTN) MANE Select	NP_001254479.2:p.Lys35380Glu
NM_003319.4:c.78943A>G (TTN)	NP_003310.4:p.Lys26315Glu
NM_133378.4:c.98434A>G (TTN)	NP_596869.4:p.Lys32812Glu
NM_133432.3:c.79318A>G (TTN)	NP_597676.3:p.Lys26440Glu
NM_133437.4:c.79519A>G (TTN)	NP_597681.4:p.Lys26507Glu
NR_038271.1:n.446+6841T>C (TTN-AS1)
NR_038272.1:n.220-5255T>C (TTN-AS1)
XM_011511729.1:c.105235A>G (TTN)	XP_011510031.1:p.Lys35079Glu
XM_011511730.1:c.79129A>G (TTN)	XP_011510032.1:p.Lys26377Glu
XM_011511731.1:c.78988A>G (TTN)	XP_011510033.1:p.Lys26330Glu
XM_017004819.1:c.105031A>G (TTN)	XP_016860308.1:p.Lys35011Glu
XM_017004820.1:c.100429A>G (TTN)	XP_016860309.1:p.Lys33477Glu
XM_017004821.1:c.100426A>G (TTN)	XP_016860310.1:p.Lys33476Glu
XM_017004822.1:c.97468A>G (TTN)	XP_016860311.1:p.Lys32490Glu
XM_017004823.1:c.79084A>G (TTN)	XP_016860312.1:p.Lys26362Glu
XM_024453094.1:c.100579A>G (TTN)	XP_024308862.1:p.Lys33527Glu
XM_024453095.1:c.100576A>G (TTN)	XP_024308863.1:p.Lys33526Glu
XM_024453096.1:c.100009A>G (TTN)	XP_024308864.1:p.Lys33337Glu
XM_024453097.1:c.97351A>G (TTN)	XP_024308865.1:p.Lys32451Glu
XM_024453098.1:c.97270A>G (TTN)	XP_024308866.1:p.Lys32424Glu
XM_024453099.1:c.79033A>G (TTN)	XP_024308867.1:p.Lys26345Glu
XM_024453100.1:c.68887A>G (TTN)	XP_024308868.1:p.Lys22963Glu