Canonical Allele Identifier: CA349406977

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395216C>A (hg19) ; chr2:g.178530489C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530489C>A , CM000664.2:g.178530489C>A	GRCh38
NC_000002.11:g.179395216C>A , CM000664.1:g.179395216C>A	GRCh37
NC_000002.10:g.179103462C>A	NCBI36
NG_011618.3:g.305314G>T , LRG_391:g.305314G>T
NG_051363.1:g.12663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98422G>T (TTN)	ENSP00000343764.6:p.Gly32808Trp
ENST00000342175.11:c.79507G>T (TTN)	ENSP00000340554.6:p.Gly26503Trp
ENST00000359218.10:c.79306G>T (TTN)	ENSP00000352154.5:p.Gly26436Trp
ENST00000342175.10:c.79507G>T (TTN)	ENSP00000340554.6:p.Gly26503Trp
ENST00000342992.10:c.98422G>T (TTN)	ENSP00000343764.6:p.Gly32808Trp
ENST00000359218.9:c.79306G>T (TTN)	ENSP00000352154.5:p.Gly26436Trp
ENST00000460472.6:c.78931G>T (TTN)	ENSP00000434586.1:p.Gly26311Trp
ENST00000589042.5:c.106126G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly35376Trp
ENST00000591111.5:c.101203G>T (TTN)	ENSP00000465570.1:p.Gly33735Trp
ENST00000615779.4:c.101203G>T (TTN)	ENSP00000483597.1:p.Gly33735Trp
NM_001256850.1:c.101203G>T (TTN)	NP_001243779.1:p.Gly33735Trp
NM_001267550.2:c.106126G>T (TTN) MANE Select	NP_001254479.2:p.Gly35376Trp
NM_003319.4:c.78931G>T (TTN)	NP_003310.4:p.Gly26311Trp
NM_133378.4:c.98422G>T (TTN)	NP_596869.4:p.Gly32808Trp
NM_133432.3:c.79306G>T (TTN)	NP_597676.3:p.Gly26436Trp
NM_133437.4:c.79507G>T (TTN)	NP_597681.4:p.Gly26503Trp
NR_038271.1:n.446+6853C>A (TTN-AS1)
NR_038272.1:n.220-5243C>A (TTN-AS1)
XM_011511729.1:c.105223G>T (TTN)	XP_011510031.1:p.Gly35075Trp
XM_011511730.1:c.79117G>T (TTN)	XP_011510032.1:p.Gly26373Trp
XM_011511731.1:c.78976G>T (TTN)	XP_011510033.1:p.Gly26326Trp
XM_017004819.1:c.105019G>T (TTN)	XP_016860308.1:p.Gly35007Trp
XM_017004820.1:c.100417G>T (TTN)	XP_016860309.1:p.Gly33473Trp
XM_017004821.1:c.100414G>T (TTN)	XP_016860310.1:p.Gly33472Trp
XM_017004822.1:c.97456G>T (TTN)	XP_016860311.1:p.Gly32486Trp
XM_017004823.1:c.79072G>T (TTN)	XP_016860312.1:p.Gly26358Trp
XM_024453094.1:c.100567G>T (TTN)	XP_024308862.1:p.Gly33523Trp
XM_024453095.1:c.100564G>T (TTN)	XP_024308863.1:p.Gly33522Trp
XM_024453096.1:c.99997G>T (TTN)	XP_024308864.1:p.Gly33333Trp
XM_024453097.1:c.97339G>T (TTN)	XP_024308865.1:p.Gly32447Trp
XM_024453098.1:c.97258G>T (TTN)	XP_024308866.1:p.Gly32420Trp
XM_024453099.1:c.79021G>T (TTN)	XP_024308867.1:p.Gly26341Trp
XM_024453100.1:c.68875G>T (TTN)	XP_024308868.1:p.Gly22959Trp