Canonical Allele Identifier: CA349646947

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179495883G>T (hg19) ; chr2:g.178631156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178631156G>T , CM000664.2:g.178631156G>T	GRCh38
NC_000002.11:g.179495883G>T , CM000664.1:g.179495883G>T	GRCh37
NC_000002.10:g.179204128G>T	NCBI36
NG_011618.3:g.204647C>A , LRG_391:g.204647C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.36188C>A	ENSP00000343764.6:p.Ala12063Asp
ENST00000342175.11:c.17273C>A	ENSP00000340554.6:p.Ala5758Asp
ENST00000359218.10:c.17072C>A	ENSP00000352154.5:p.Ala5691Asp
ENST00000342175.10:c.17273C>A	ENSP00000340554.6:p.Ala5758Asp
ENST00000342992.10:c.36188C>A	ENSP00000343764.6:p.Ala12063Asp
ENST00000359218.9:c.17072C>A	ENSP00000352154.5:p.Ala5691Asp
ENST00000460472.6:c.16697C>A	ENSP00000434586.1:p.Ala5566Asp
ENST00000589042.5:c.43892C>A MANE Select	ENSP00000467141.1:p.Ala14631Asp
ENST00000591111.5:c.38969C>A	ENSP00000465570.1:p.Ala12990Asp
ENST00000615779.4:c.38969C>A	ENSP00000483597.1:p.Ala12990Asp
NM_001256850.1:c.38969C>A	NP_001243779.1:p.Ala12990Asp
NM_001267550.2:c.43892C>A MANE Select	NP_001254479.2:p.Ala14631Asp
NM_003319.4:c.16697C>A	NP_003310.4:p.Ala5566Asp
NM_133378.4:c.36188C>A	NP_596869.4:p.Ala12063Asp
NM_133432.3:c.17072C>A	NP_597676.3:p.Ala5691Asp
NM_133437.4:c.17273C>A	NP_597681.4:p.Ala5758Asp
XM_011511729.1:c.42989C>A	XP_011510031.1:p.Ala14330Asp
XM_011511730.1:c.16883C>A	XP_011510032.1:p.Ala5628Asp
XM_011511731.1:c.16742C>A	XP_011510033.1:p.Ala5581Asp
XM_017004819.1:c.42785C>A	XP_016860308.1:p.Ala14262Asp
XM_017004820.1:c.38183C>A	XP_016860309.1:p.Ala12728Asp
XM_017004821.1:c.38180C>A	XP_016860310.1:p.Ala12727Asp
XM_017004822.1:c.35222C>A	XP_016860311.1:p.Ala11741Asp
XM_017004823.1:c.16838C>A	XP_016860312.1:p.Ala5613Asp
XM_024453094.1:c.38333C>A	XP_024308862.1:p.Ala12778Asp
XM_024453095.1:c.38330C>A	XP_024308863.1:p.Ala12777Asp
XM_024453096.1:c.37763C>A	XP_024308864.1:p.Ala12588Asp
XM_024453097.1:c.35105C>A	XP_024308865.1:p.Ala11702Asp
XM_024453098.1:c.35024C>A	XP_024308866.1:p.Ala11675Asp
XM_024453099.1:c.16787C>A	XP_024308867.1:p.Ala5596Asp
XM_024453100.1:c.6641C>A	XP_024308868.1:p.Ala2214Asp