Canonical Allele Identifier: CA1310514670

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530482G= , CM000664.2:g.178530482G=	GRCh38
NC_000002.11:g.179395209G= , CM000664.1:g.179395209G=	GRCh37
NC_000002.10:g.179103455G=	NCBI36
NG_011618.3:g.305321C= , LRG_391:g.305321C=
NG_051363.1:g.12656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98429C= (TTN)	ENSP00000343764.6:p.Ala32810=
ENST00000342175.11:c.79514C= (TTN)	ENSP00000340554.6:p.Ala26505=
ENST00000359218.10:c.79313C= (TTN)	ENSP00000352154.5:p.Ala26438=
ENST00000342175.10:c.79514C= (TTN)	ENSP00000340554.6:p.Ala26505=
ENST00000342992.10:c.98429C= (TTN)	ENSP00000343764.6:p.Ala32810=
ENST00000359218.9:c.79313C= (TTN)	ENSP00000352154.5:p.Ala26438=
ENST00000460472.6:c.78938C= (TTN)	ENSP00000434586.1:p.Ala26313=
ENST00000589042.5:c.106133C= (TTN) MANE Select	ENSP00000467141.1:p.Ala35378=
ENST00000591111.5:c.101210C= (TTN)	ENSP00000465570.1:p.Ala33737=
ENST00000615779.4:c.101210C= (TTN)	ENSP00000483597.1:p.Ala33737=
NM_001256850.1:c.101210C= (TTN)	NP_001243779.1:p.Ala33737=
NM_001267550.2:c.106133C= (TTN) MANE Select	NP_001254479.2:p.Ala35378=
NM_003319.4:c.78938C= (TTN)	NP_003310.4:p.Ala26313=
NM_133378.4:c.98429C= (TTN)	NP_596869.4:p.Ala32810=
NM_133432.3:c.79313C= (TTN)	NP_597676.3:p.Ala26438=
NM_133437.4:c.79514C= (TTN)	NP_597681.4:p.Ala26505=
NR_038271.1:n.446+6846G= (TTN-AS1)
NR_038272.1:n.220-5250G= (TTN-AS1)
XM_011511729.1:c.105230C= (TTN)	XP_011510031.1:p.Ala35077=
XM_011511730.1:c.79124C= (TTN)	XP_011510032.1:p.Ala26375=
XM_011511731.1:c.78983C= (TTN)	XP_011510033.1:p.Ala26328=
XM_017004819.1:c.105026C= (TTN)	XP_016860308.1:p.Ala35009=
XM_017004820.1:c.100424C= (TTN)	XP_016860309.1:p.Ala33475=
XM_017004821.1:c.100421C= (TTN)	XP_016860310.1:p.Ala33474=
XM_017004822.1:c.97463C= (TTN)	XP_016860311.1:p.Ala32488=
XM_017004823.1:c.79079C= (TTN)	XP_016860312.1:p.Ala26360=
XM_024453094.1:c.100574C= (TTN)	XP_024308862.1:p.Ala33525=
XM_024453095.1:c.100571C= (TTN)	XP_024308863.1:p.Ala33524=
XM_024453096.1:c.100004C= (TTN)	XP_024308864.1:p.Ala33335=
XM_024453097.1:c.97346C= (TTN)	XP_024308865.1:p.Ala32449=
XM_024453098.1:c.97265C= (TTN)	XP_024308866.1:p.Ala32422=
XM_024453099.1:c.79028C= (TTN)	XP_024308867.1:p.Ala26343=
XM_024453100.1:c.68882C= (TTN)	XP_024308868.1:p.Ala22961=