Canonical Allele Identifier: CA349434876

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179404797A>G (hg19) ; chr2:g.178540070A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178540070A>G , CM000664.2:g.178540070A>G	GRCh38
NC_000002.11:g.179404797A>G , CM000664.1:g.179404797A>G	GRCh37
NC_000002.10:g.179113043A>G	NCBI36
NG_011618.3:g.295733T>C , LRG_391:g.295733T>C
NG_051363.1:g.22244A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.90392T>C (TTN)	ENSP00000343764.6:p.Leu30131Pro
ENST00000342175.11:c.71477T>C (TTN)	ENSP00000340554.6:p.Leu23826Pro
ENST00000359218.10:c.71276T>C (TTN)	ENSP00000352154.5:p.Leu23759Pro
ENST00000342175.10:c.71477T>C (TTN)	ENSP00000340554.6:p.Leu23826Pro
ENST00000342992.10:c.90392T>C (TTN)	ENSP00000343764.6:p.Leu30131Pro
ENST00000359218.9:c.71276T>C (TTN)	ENSP00000352154.5:p.Leu23759Pro
ENST00000460472.6:c.70901T>C (TTN)	ENSP00000434586.1:p.Leu23634Pro
ENST00000589042.5:c.98096T>C (TTN) MANE Select	ENSP00000467141.1:p.Leu32699Pro
ENST00000591111.5:c.93173T>C (TTN)	ENSP00000465570.1:p.Leu31058Pro
ENST00000615779.4:c.93173T>C (TTN)	ENSP00000483597.1:p.Leu31058Pro
NM_001256850.1:c.93173T>C (TTN)	NP_001243779.1:p.Leu31058Pro
NM_001267550.2:c.98096T>C (TTN) MANE Select	NP_001254479.2:p.Leu32699Pro
NM_003319.4:c.70901T>C (TTN)	NP_003310.4:p.Leu23634Pro
NM_133378.4:c.90392T>C (TTN)	NP_596869.4:p.Leu30131Pro
NM_133432.3:c.71276T>C (TTN)	NP_597676.3:p.Leu23759Pro
NM_133437.4:c.71477T>C (TTN)	NP_597681.4:p.Leu23826Pro
NR_038271.1:n.446+16434A>G (TTN-AS1)
NR_038272.1:n.1841-37A>G (TTN-AS1)
XM_011511729.1:c.97193T>C (TTN)	XP_011510031.1:p.Leu32398Pro
XM_011511730.1:c.71087T>C (TTN)	XP_011510032.1:p.Leu23696Pro
XM_011511731.1:c.70946T>C (TTN)	XP_011510033.1:p.Leu23649Pro
XM_017004819.1:c.96989T>C (TTN)	XP_016860308.1:p.Leu32330Pro
XM_017004820.1:c.92387T>C (TTN)	XP_016860309.1:p.Leu30796Pro
XM_017004821.1:c.92384T>C (TTN)	XP_016860310.1:p.Leu30795Pro
XM_017004822.1:c.89426T>C (TTN)	XP_016860311.1:p.Leu29809Pro
XM_017004823.1:c.71042T>C (TTN)	XP_016860312.1:p.Leu23681Pro
XM_024453094.1:c.92537T>C (TTN)	XP_024308862.1:p.Leu30846Pro
XM_024453095.1:c.92534T>C (TTN)	XP_024308863.1:p.Leu30845Pro
XM_024453096.1:c.91967T>C (TTN)	XP_024308864.1:p.Leu30656Pro
XM_024453097.1:c.89309T>C (TTN)	XP_024308865.1:p.Leu29770Pro
XM_024453098.1:c.89228T>C (TTN)	XP_024308866.1:p.Leu29743Pro
XM_024453099.1:c.70991T>C (TTN)	XP_024308867.1:p.Leu23664Pro
XM_024453100.1:c.60845T>C (TTN)	XP_024308868.1:p.Leu20282Pro