Canonical Allele Identifier: CA1310546582

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607484A= , CM000664.2:g.178607484A=	GRCh38
NC_000002.11:g.179472211A= , CM000664.1:g.179472211A=	GRCh37
NC_000002.10:g.179180456A=	NCBI36
NG_011618.3:g.228319T= , LRG_391:g.228319T=
NG_051363.1:g.89658A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45500T= (TTN)	ENSP00000343764.6:p.Leu15167=
ENST00000342175.11:c.26585T= (TTN)	ENSP00000340554.6:p.Leu8862=
ENST00000359218.10:c.26384T= (TTN)	ENSP00000352154.5:p.Leu8795=
ENST00000342175.10:c.26585T= (TTN)	ENSP00000340554.6:p.Leu8862=
ENST00000342992.10:c.45500T= (TTN)	ENSP00000343764.6:p.Leu15167=
ENST00000359218.9:c.26384T= (TTN)	ENSP00000352154.5:p.Leu8795=
ENST00000460472.6:c.26009T= (TTN)	ENSP00000434586.1:p.Leu8670=
ENST00000589042.5:c.53204T= (TTN) MANE Select	ENSP00000467141.1:p.Leu17735=
ENST00000591111.5:c.48281T= (TTN)	ENSP00000465570.1:p.Leu16094=
ENST00000615779.4:c.48281T= (TTN)	ENSP00000483597.1:p.Leu16094=
NM_001256850.1:c.48281T= (TTN)	NP_001243779.1:p.Leu16094=
NM_001267550.2:c.53204T= (TTN) MANE Select	NP_001254479.2:p.Leu17735=
NM_003319.4:c.26009T= (TTN)	NP_003310.4:p.Leu8670=
NM_133378.4:c.45500T= (TTN)	NP_596869.4:p.Leu15167=
NM_133432.3:c.26384T= (TTN)	NP_597676.3:p.Leu8795=
NM_133437.4:c.26585T= (TTN)	NP_597681.4:p.Leu8862=
NR_038271.1:n.683-683A= (TTN-AS1)
XM_011511729.1:c.52301T= (TTN)	XP_011510031.1:p.Leu17434=
XM_011511730.1:c.26195T= (TTN)	XP_011510032.1:p.Leu8732=
XM_011511731.1:c.26054T= (TTN)	XP_011510033.1:p.Leu8685=
XM_017004819.1:c.52097T= (TTN)	XP_016860308.1:p.Leu17366=
XM_017004820.1:c.47495T= (TTN)	XP_016860309.1:p.Leu15832=
XM_017004821.1:c.47492T= (TTN)	XP_016860310.1:p.Leu15831=
XM_017004822.1:c.44534T= (TTN)	XP_016860311.1:p.Leu14845=
XM_017004823.1:c.26150T= (TTN)	XP_016860312.1:p.Leu8717=
XM_024453094.1:c.47645T= (TTN)	XP_024308862.1:p.Leu15882=
XM_024453095.1:c.47642T= (TTN)	XP_024308863.1:p.Leu15881=
XM_024453096.1:c.47075T= (TTN)	XP_024308864.1:p.Leu15692=
XM_024453097.1:c.44417T= (TTN)	XP_024308865.1:p.Leu14806=
XM_024453098.1:c.44336T= (TTN)	XP_024308866.1:p.Leu14779=
XM_024453099.1:c.26099T= (TTN)	XP_024308867.1:p.Leu8700=
XM_024453100.1:c.15953T= (TTN)	XP_024308868.1:p.Leu5318=