Canonical Allele Identifier: CA349541202

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179466274T>G (hg19) ; chr2:g.178601547T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178601547T>G , CM000664.2:g.178601547T>G	GRCh38
NC_000002.11:g.179466274T>G , CM000664.1:g.179466274T>G	GRCh37
NC_000002.10:g.179174519T>G	NCBI36
NG_011618.3:g.234256A>C , LRG_391:g.234256A>C
NG_051363.1:g.83721T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.47746A>C (TTN)	ENSP00000343764.6:p.Lys15916Gln
ENST00000342175.11:c.28831A>C (TTN)	ENSP00000340554.6:p.Lys9611Gln
ENST00000359218.10:c.28630A>C (TTN)	ENSP00000352154.5:p.Lys9544Gln
ENST00000342175.10:c.28831A>C (TTN)	ENSP00000340554.6:p.Lys9611Gln
ENST00000342992.10:c.47746A>C (TTN)	ENSP00000343764.6:p.Lys15916Gln
ENST00000359218.9:c.28630A>C (TTN)	ENSP00000352154.5:p.Lys9544Gln
ENST00000460472.6:c.28255A>C (TTN)	ENSP00000434586.1:p.Lys9419Gln
ENST00000589042.5:c.55450A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys18484Gln
ENST00000591111.5:c.50527A>C (TTN)	ENSP00000465570.1:p.Lys16843Gln
ENST00000615779.4:c.50527A>C (TTN)	ENSP00000483597.1:p.Lys16843Gln
NM_001256850.1:c.50527A>C (TTN)	NP_001243779.1:p.Lys16843Gln
NM_001267550.2:c.55450A>C (TTN) MANE Select	NP_001254479.2:p.Lys18484Gln
NM_003319.4:c.28255A>C (TTN)	NP_003310.4:p.Lys9419Gln
NM_133378.4:c.47746A>C (TTN)	NP_596869.4:p.Lys15916Gln
NM_133432.3:c.28630A>C (TTN)	NP_597676.3:p.Lys9544Gln
NM_133437.4:c.28831A>C (TTN)	NP_597681.4:p.Lys9611Gln
NR_038271.1:n.682+3866T>G (TTN-AS1)
NR_038272.1:n.3917+880T>G (TTN-AS1)
XM_011511729.1:c.54547A>C (TTN)	XP_011510031.1:p.Lys18183Gln
XM_011511730.1:c.28441A>C (TTN)	XP_011510032.1:p.Lys9481Gln
XM_011511731.1:c.28300A>C (TTN)	XP_011510033.1:p.Lys9434Gln
XM_017004819.1:c.54343A>C (TTN)	XP_016860308.1:p.Lys18115Gln
XM_017004820.1:c.49741A>C (TTN)	XP_016860309.1:p.Lys16581Gln
XM_017004821.1:c.49738A>C (TTN)	XP_016860310.1:p.Lys16580Gln
XM_017004822.1:c.46780A>C (TTN)	XP_016860311.1:p.Lys15594Gln
XM_017004823.1:c.28396A>C (TTN)	XP_016860312.1:p.Lys9466Gln
XM_024453094.1:c.49891A>C (TTN)	XP_024308862.1:p.Lys16631Gln
XM_024453095.1:c.49888A>C (TTN)	XP_024308863.1:p.Lys16630Gln
XM_024453096.1:c.49321A>C (TTN)	XP_024308864.1:p.Lys16441Gln
XM_024453097.1:c.46663A>C (TTN)	XP_024308865.1:p.Lys15555Gln
XM_024453098.1:c.46582A>C (TTN)	XP_024308866.1:p.Lys15528Gln
XM_024453099.1:c.28345A>C (TTN)	XP_024308867.1:p.Lys9449Gln
XM_024453100.1:c.18199A>C (TTN)	XP_024308868.1:p.Lys6067Gln