Canonical Allele Identifier: CA349647811

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179438602T>G (hg19) ; chr2:g.178573875T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178573875T>G , CM000664.2:g.178573875T>G	GRCh38
NC_000002.11:g.179438602T>G , CM000664.1:g.179438602T>G	GRCh37
NC_000002.10:g.179146848T>G	NCBI36
NG_011618.3:g.261928A>C , LRG_391:g.261928A>C
NG_051363.1:g.56049T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.64553A>C (TTN)	ENSP00000343764.6:p.Asn21518Thr
ENST00000342175.11:c.45638A>C (TTN)	ENSP00000340554.6:p.Asn15213Thr
ENST00000359218.10:c.45437A>C (TTN)	ENSP00000352154.5:p.Asn15146Thr
ENST00000342175.10:c.45638A>C (TTN)	ENSP00000340554.6:p.Asn15213Thr
ENST00000342992.10:c.64553A>C (TTN)	ENSP00000343764.6:p.Asn21518Thr
ENST00000359218.9:c.45437A>C (TTN)	ENSP00000352154.5:p.Asn15146Thr
ENST00000460472.6:c.45062A>C (TTN)	ENSP00000434586.1:p.Asn15021Thr
ENST00000589042.5:c.72257A>C (TTN) MANE Select	ENSP00000467141.1:p.Asn24086Thr
ENST00000591111.5:c.67334A>C (TTN)	ENSP00000465570.1:p.Asn22445Thr
ENST00000615779.4:c.67334A>C (TTN)	ENSP00000483597.1:p.Asn22445Thr
NM_001256850.1:c.67334A>C (TTN)	NP_001243779.1:p.Asn22445Thr
NM_001267550.2:c.72257A>C (TTN) MANE Select	NP_001254479.2:p.Asn24086Thr
NM_003319.4:c.45062A>C (TTN)	NP_003310.4:p.Asn15021Thr
NM_133378.4:c.64553A>C (TTN)	NP_596869.4:p.Asn21518Thr
NM_133432.3:c.45437A>C (TTN)	NP_597676.3:p.Asn15146Thr
NM_133437.4:c.45638A>C (TTN)	NP_597681.4:p.Asn15213Thr
NR_038271.1:n.596+2426T>G (TTN-AS1)
NR_038272.1:n.2044-8697T>G (TTN-AS1)
XM_011511729.1:c.71354A>C (TTN)	XP_011510031.1:p.Asn23785Thr
XM_011511730.1:c.45248A>C (TTN)	XP_011510032.1:p.Asn15083Thr
XM_011511731.1:c.45107A>C (TTN)	XP_011510033.1:p.Asn15036Thr
XM_017004819.1:c.71150A>C (TTN)	XP_016860308.1:p.Asn23717Thr
XM_017004820.1:c.66548A>C (TTN)	XP_016860309.1:p.Asn22183Thr
XM_017004821.1:c.66545A>C (TTN)	XP_016860310.1:p.Asn22182Thr
XM_017004822.1:c.63587A>C (TTN)	XP_016860311.1:p.Asn21196Thr
XM_017004823.1:c.45203A>C (TTN)	XP_016860312.1:p.Asn15068Thr
XM_024453094.1:c.66698A>C (TTN)	XP_024308862.1:p.Asn22233Thr
XM_024453095.1:c.66695A>C (TTN)	XP_024308863.1:p.Asn22232Thr
XM_024453096.1:c.66128A>C (TTN)	XP_024308864.1:p.Asn22043Thr
XM_024453097.1:c.63470A>C (TTN)	XP_024308865.1:p.Asn21157Thr
XM_024453098.1:c.63389A>C (TTN)	XP_024308866.1:p.Asn21130Thr
XM_024453099.1:c.45152A>C (TTN)	XP_024308867.1:p.Asn15051Thr
XM_024453100.1:c.35006A>C (TTN)	XP_024308868.1:p.Asn11669Thr