Canonical Allele Identifier: CA60976857

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178599849G>T , CM000664.2:g.178599849G>T	GRCh38
NC_000002.11:g.179464576G>T , CM000664.1:g.179464576G>T	GRCh37
NC_000002.10:g.179172821G>T	NCBI36
NG_011618.3:g.235954C>A , LRG_391:g.235954C>A
NG_051363.1:g.82023G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.56052C>A (TTN) MANE Select	NP_001254479.2:p.Cys18684Ter
ENST00000589042.5:c.56052C>A (TTN) MANE Select	ENSP00000467141.1:p.Cys18684Ter
NM_001256850.1:c.51129C>A (TTN)	NP_001243779.1:p.Cys17043Ter
NM_003319.4:c.28857C>A (TTN)	NP_003310.4:p.Cys9619Ter
NM_133378.4:c.48348C>A (TTN)	NP_596869.4:p.Cys16116Ter
NM_133432.3:c.29232C>A (TTN)	NP_597676.3:p.Cys9744Ter
NM_133437.4:c.29433C>A (TTN)	NP_597681.4:p.Cys9811Ter
NR_038271.1:n.682+2168G>T (TTN-AS1)
NR_038272.1:n.3725+99G>T (TTN-AS1)
ENST00000342175.10:c.29433C>A (TTN)	ENSP00000340554.6:p.Cys9811Ter
ENST00000342175.11:c.29433C>A (TTN)	ENSP00000340554.6:p.Cys9811Ter
ENST00000342992.10:c.48348C>A (TTN)	ENSP00000343764.6:p.Cys16116Ter
ENST00000342992.11:c.48348C>A (TTN)	ENSP00000343764.6:p.Cys16116Ter
ENST00000359218.10:c.29232C>A (TTN)	ENSP00000352154.5:p.Cys9744Ter
ENST00000359218.9:c.29232C>A (TTN)	ENSP00000352154.5:p.Cys9744Ter
ENST00000460472.6:c.28857C>A (TTN)	ENSP00000434586.1:p.Cys9619Ter
ENST00000591111.5:c.51129C>A (TTN)	ENSP00000465570.1:p.Cys17043Ter
ENST00000615779.4:c.51129C>A (TTN)	ENSP00000483597.1:p.Cys17043Ter
XM_011511729.1:c.55149C>A (TTN)	XP_011510031.1:p.Cys18383Ter
XM_011511730.1:c.29043C>A (TTN)	XP_011510032.1:p.Cys9681Ter
XM_011511731.1:c.28902C>A (TTN)	XP_011510033.1:p.Cys9634Ter
XM_017004819.1:c.54945C>A (TTN)	XP_016860308.1:p.Cys18315Ter
XM_017004820.1:c.50343C>A (TTN)	XP_016860309.1:p.Cys16781Ter
XM_017004821.1:c.50340C>A (TTN)	XP_016860310.1:p.Cys16780Ter
XM_017004822.1:c.47382C>A (TTN)	XP_016860311.1:p.Cys15794Ter
XM_017004823.1:c.28998C>A (TTN)	XP_016860312.1:p.Cys9666Ter
XM_024453094.1:c.50493C>A (TTN)	XP_024308862.1:p.Cys16831Ter
XM_024453095.1:c.50490C>A (TTN)	XP_024308863.1:p.Cys16830Ter
XM_024453096.1:c.49923C>A (TTN)	XP_024308864.1:p.Cys16641Ter
XM_024453097.1:c.47265C>A (TTN)	XP_024308865.1:p.Cys15755Ter
XM_024453098.1:c.47184C>A (TTN)	XP_024308866.1:p.Cys15728Ter
XM_024453099.1:c.28947C>A (TTN)	XP_024308867.1:p.Cys9649Ter
XM_024453100.1:c.18801C>A (TTN)	XP_024308868.1:p.Cys6267Ter