Canonical Allele Identifier: CA349602102

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179602881A>C (hg19) ; chr2:g.178738154A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178738154A>C , CM000664.2:g.178738154A>C	GRCh38
NC_000002.11:g.179602881A>C , CM000664.1:g.179602881A>C	GRCh37
NC_000002.10:g.179311126A>C	NCBI36
NG_011618.3:g.97649T>G , LRG_391:g.97649T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.10567T>G	ENSP00000343764.6:p.Cys3523Gly
ENST00000342175.11:c.13786T>G	ENSP00000340554.6:p.Cys4596Gly
ENST00000359218.10:c.13585T>G	ENSP00000352154.5:p.Cys4529Gly
ENST00000342175.10:c.13786T>G	ENSP00000340554.6:p.Cys4596Gly
ENST00000342992.10:c.10567T>G	ENSP00000343764.6:p.Cys3523Gly
ENST00000359218.9:c.13585T>G	ENSP00000352154.5:p.Cys4529Gly
ENST00000460472.6:c.13210T>G	ENSP00000434586.1:p.Cys4404Gly
ENST00000589042.5:c.14299T>G MANE Select	ENSP00000467141.1:p.Cys4767Gly
ENST00000591111.5:c.13348T>G	ENSP00000465570.1:p.Cys4450Gly
ENST00000615779.4:c.13348T>G	ENSP00000483597.1:p.Cys4450Gly
NM_001256850.1:c.13348T>G	NP_001243779.1:p.Cys4450Gly
NM_001267550.2:c.14299T>G MANE Select	NP_001254479.2:p.Cys4767Gly
NM_003319.4:c.13210T>G	NP_003310.4:p.Cys4404Gly
NM_133378.4:c.10567T>G	NP_596869.4:p.Cys3523Gly
NM_133432.3:c.13585T>G	NP_597676.3:p.Cys4529Gly
NM_133437.4:c.13786T>G	NP_597681.4:p.Cys4596Gly
XM_011511729.1:c.13396T>G	XP_011510031.1:p.Cys4466Gly
XM_011511730.1:c.13396T>G	XP_011510032.1:p.Cys4466Gly
XM_011511731.1:c.13255T>G	XP_011510033.1:p.Cys4419Gly
XM_017004819.1:c.13351T>G	XP_016860308.1:p.Cys4451Gly
XM_017004820.1:c.10570T>G	XP_016860309.1:p.Cys3524Gly
XM_017004821.1:c.10567T>G	XP_016860310.1:p.Cys3523Gly
XM_017004822.1:c.13351T>G	XP_016860311.1:p.Cys4451Gly
XM_017004823.1:c.13351T>G	XP_016860312.1:p.Cys4451Gly
XM_024453094.1:c.13351T>G	XP_024308862.1:p.Cys4451Gly
XM_024453095.1:c.13351T>G	XP_024308863.1:p.Cys4451Gly
XM_024453096.1:c.13351T>G	XP_024308864.1:p.Cys4451Gly
XM_024453097.1:c.13351T>G	XP_024308865.1:p.Cys4451Gly
XM_024453098.1:c.13351T>G	XP_024308866.1:p.Cys4451Gly
XM_024453099.1:c.13351T>G	XP_024308867.1:p.Cys4451Gly