Canonical Allele Identifier: CA1310514647

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530465C= , CM000664.2:g.178530465C=	GRCh38
NC_000002.11:g.179395192C= , CM000664.1:g.179395192C=	GRCh37
NC_000002.10:g.179103438C=	NCBI36
NG_011618.3:g.305338G= , LRG_391:g.305338G=
NG_051363.1:g.12639C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98446G= (TTN)	ENSP00000343764.6:p.Glu32816=
ENST00000342175.11:c.79531G= (TTN)	ENSP00000340554.6:p.Glu26511=
ENST00000359218.10:c.79330G= (TTN)	ENSP00000352154.5:p.Glu26444=
ENST00000342175.10:c.79531G= (TTN)	ENSP00000340554.6:p.Glu26511=
ENST00000342992.10:c.98446G= (TTN)	ENSP00000343764.6:p.Glu32816=
ENST00000359218.9:c.79330G= (TTN)	ENSP00000352154.5:p.Glu26444=
ENST00000460472.6:c.78955G= (TTN)	ENSP00000434586.1:p.Glu26319=
ENST00000589042.5:c.106150G= (TTN) MANE Select	ENSP00000467141.1:p.Glu35384=
ENST00000591111.5:c.101227G= (TTN)	ENSP00000465570.1:p.Glu33743=
ENST00000615779.4:c.101227G= (TTN)	ENSP00000483597.1:p.Glu33743=
NM_001256850.1:c.101227G= (TTN)	NP_001243779.1:p.Glu33743=
NM_001267550.2:c.106150G= (TTN) MANE Select	NP_001254479.2:p.Glu35384=
NM_003319.4:c.78955G= (TTN)	NP_003310.4:p.Glu26319=
NM_133378.4:c.98446G= (TTN)	NP_596869.4:p.Glu32816=
NM_133432.3:c.79330G= (TTN)	NP_597676.3:p.Glu26444=
NM_133437.4:c.79531G= (TTN)	NP_597681.4:p.Glu26511=
NR_038271.1:n.446+6829C= (TTN-AS1)
NR_038272.1:n.220-5267C= (TTN-AS1)
XM_011511729.1:c.105247G= (TTN)	XP_011510031.1:p.Glu35083=
XM_011511730.1:c.79141G= (TTN)	XP_011510032.1:p.Glu26381=
XM_011511731.1:c.79000G= (TTN)	XP_011510033.1:p.Glu26334=
XM_017004819.1:c.105043G= (TTN)	XP_016860308.1:p.Glu35015=
XM_017004820.1:c.100441G= (TTN)	XP_016860309.1:p.Glu33481=
XM_017004821.1:c.100438G= (TTN)	XP_016860310.1:p.Glu33480=
XM_017004822.1:c.97480G= (TTN)	XP_016860311.1:p.Glu32494=
XM_017004823.1:c.79096G= (TTN)	XP_016860312.1:p.Glu26366=
XM_024453094.1:c.100591G= (TTN)	XP_024308862.1:p.Glu33531=
XM_024453095.1:c.100588G= (TTN)	XP_024308863.1:p.Glu33530=
XM_024453096.1:c.100021G= (TTN)	XP_024308864.1:p.Glu33341=
XM_024453097.1:c.97363G= (TTN)	XP_024308865.1:p.Glu32455=
XM_024453098.1:c.97282G= (TTN)	XP_024308866.1:p.Glu32428=
XM_024453099.1:c.79045G= (TTN)	XP_024308867.1:p.Glu26349=
XM_024453100.1:c.68899G= (TTN)	XP_024308868.1:p.Glu22967=