Canonical Allele Identifier: CA1986927

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178545548C>G , CM000664.2:g.178545548C>G	GRCh38
NC_000002.11:g.179410275C>G , CM000664.1:g.179410275C>G	GRCh37
NC_000002.10:g.179118521C>G	NCBI36
NG_011618.3:g.290255G>C , LRG_391:g.290255G>C
NG_051363.1:g.27722C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.95562G>C (TTN) MANE Select	NP_001254479.2:p.Trp31854Cys
ENST00000589042.5:c.95562G>C (TTN) MANE Select	ENSP00000467141.1:p.Trp31854Cys
NM_001256850.1:c.90639G>C (TTN)	NP_001243779.1:p.Trp30213Cys
NM_003319.4:c.68367G>C (TTN)	NP_003310.4:p.Trp22789Cys
NM_133378.4:c.87858G>C (TTN)	NP_596869.4:p.Trp29286Cys
NM_133432.3:c.68742G>C (TTN)	NP_597676.3:p.Trp22914Cys
NM_133437.4:c.68943G>C (TTN)	NP_597681.4:p.Trp22981Cys
NR_038271.1:n.446+21912C>G (TTN-AS1)
NR_038272.1:n.2043+3187C>G (TTN-AS1)
ENST00000342175.10:c.68943G>C (TTN)	ENSP00000340554.6:p.Trp22981Cys
ENST00000342175.11:c.68943G>C (TTN)	ENSP00000340554.6:p.Trp22981Cys
ENST00000342992.10:c.87858G>C (TTN)	ENSP00000343764.6:p.Trp29286Cys
ENST00000342992.11:c.87858G>C (TTN)	ENSP00000343764.6:p.Trp29286Cys
ENST00000359218.10:c.68742G>C (TTN)	ENSP00000352154.5:p.Trp22914Cys
ENST00000359218.9:c.68742G>C (TTN)	ENSP00000352154.5:p.Trp22914Cys
ENST00000460472.6:c.68367G>C (TTN)	ENSP00000434586.1:p.Trp22789Cys
ENST00000591111.5:c.90639G>C (TTN)	ENSP00000465570.1:p.Trp30213Cys
ENST00000615779.4:c.90639G>C (TTN)	ENSP00000483597.1:p.Trp30213Cys
XM_011511729.1:c.94659G>C (TTN)	XP_011510031.1:p.Trp31553Cys
XM_011511730.1:c.68553G>C (TTN)	XP_011510032.1:p.Trp22851Cys
XM_011511731.1:c.68412G>C (TTN)	XP_011510033.1:p.Trp22804Cys
XM_017004819.1:c.94455G>C (TTN)	XP_016860308.1:p.Trp31485Cys
XM_017004820.1:c.89853G>C (TTN)	XP_016860309.1:p.Trp29951Cys
XM_017004821.1:c.89850G>C (TTN)	XP_016860310.1:p.Trp29950Cys
XM_017004822.1:c.86892G>C (TTN)	XP_016860311.1:p.Trp28964Cys
XM_017004823.1:c.68508G>C (TTN)	XP_016860312.1:p.Trp22836Cys
XM_024453094.1:c.90003G>C (TTN)	XP_024308862.1:p.Trp30001Cys
XM_024453095.1:c.90000G>C (TTN)	XP_024308863.1:p.Trp30000Cys
XM_024453096.1:c.89433G>C (TTN)	XP_024308864.1:p.Trp29811Cys
XM_024453097.1:c.86775G>C (TTN)	XP_024308865.1:p.Trp28925Cys
XM_024453098.1:c.86694G>C (TTN)	XP_024308866.1:p.Trp28898Cys
XM_024453099.1:c.68457G>C (TTN)	XP_024308867.1:p.Trp22819Cys
XM_024453100.1:c.58311G>C (TTN)	XP_024308868.1:p.Trp19437Cys