Canonical Allele Identifier: CA349645678

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179495067T>C (hg19) ; chr2:g.178630340T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630340T>C , CM000664.2:g.178630340T>C	GRCh38
NC_000002.11:g.179495067T>C , CM000664.1:g.179495067T>C	GRCh37
NC_000002.10:g.179203312T>C	NCBI36
NG_011618.3:g.205463A>G , LRG_391:g.205463A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36478A>G	ENSP00000343764.6:p.Ile12160Val
ENST00000342175.11:c.17563A>G	ENSP00000340554.6:p.Ile5855Val
ENST00000359218.10:c.17362A>G	ENSP00000352154.5:p.Ile5788Val
ENST00000342175.10:c.17563A>G	ENSP00000340554.6:p.Ile5855Val
ENST00000342992.10:c.36478A>G	ENSP00000343764.6:p.Ile12160Val
ENST00000359218.9:c.17362A>G	ENSP00000352154.5:p.Ile5788Val
ENST00000460472.6:c.16987A>G	ENSP00000434586.1:p.Ile5663Val
ENST00000589042.5:c.44182A>G MANE Select	ENSP00000467141.1:p.Ile14728Val
ENST00000591111.5:c.39259A>G	ENSP00000465570.1:p.Ile13087Val
ENST00000615779.4:c.39259A>G	ENSP00000483597.1:p.Ile13087Val
NM_001256850.1:c.39259A>G	NP_001243779.1:p.Ile13087Val
NM_001267550.2:c.44182A>G MANE Select	NP_001254479.2:p.Ile14728Val
NM_003319.4:c.16987A>G	NP_003310.4:p.Ile5663Val
NM_133378.4:c.36478A>G	NP_596869.4:p.Ile12160Val
NM_133432.3:c.17362A>G	NP_597676.3:p.Ile5788Val
NM_133437.4:c.17563A>G	NP_597681.4:p.Ile5855Val
XM_011511729.1:c.43279A>G	XP_011510031.1:p.Ile14427Val
XM_011511730.1:c.17173A>G	XP_011510032.1:p.Ile5725Val
XM_011511731.1:c.17032A>G	XP_011510033.1:p.Ile5678Val
XM_017004819.1:c.43075A>G	XP_016860308.1:p.Ile14359Val
XM_017004820.1:c.38473A>G	XP_016860309.1:p.Ile12825Val
XM_017004821.1:c.38470A>G	XP_016860310.1:p.Ile12824Val
XM_017004822.1:c.35512A>G	XP_016860311.1:p.Ile11838Val
XM_017004823.1:c.17128A>G	XP_016860312.1:p.Ile5710Val
XM_024453094.1:c.38623A>G	XP_024308862.1:p.Ile12875Val
XM_024453095.1:c.38620A>G	XP_024308863.1:p.Ile12874Val
XM_024453096.1:c.38053A>G	XP_024308864.1:p.Ile12685Val
XM_024453097.1:c.35395A>G	XP_024308865.1:p.Ile11799Val
XM_024453098.1:c.35314A>G	XP_024308866.1:p.Ile11772Val
XM_024453099.1:c.17077A>G	XP_024308867.1:p.Ile5693Val
XM_024453100.1:c.6931A>G	XP_024308868.1:p.Ile2311Val