Canonical Allele Identifier: CA1310514697

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530503T= , CM000664.2:g.178530503T=	GRCh38
NC_000002.11:g.179395230T= , CM000664.1:g.179395230T=	GRCh37
NC_000002.10:g.179103476T=	NCBI36
NG_011618.3:g.305300A= , LRG_391:g.305300A=
NG_051363.1:g.12677T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98408A= (TTN)	ENSP00000343764.6:p.Asn32803=
ENST00000342175.11:c.79493A= (TTN)	ENSP00000340554.6:p.Asn26498=
ENST00000359218.10:c.79292A= (TTN)	ENSP00000352154.5:p.Asn26431=
ENST00000342175.10:c.79493A= (TTN)	ENSP00000340554.6:p.Asn26498=
ENST00000342992.10:c.98408A= (TTN)	ENSP00000343764.6:p.Asn32803=
ENST00000359218.9:c.79292A= (TTN)	ENSP00000352154.5:p.Asn26431=
ENST00000460472.6:c.78917A= (TTN)	ENSP00000434586.1:p.Asn26306=
ENST00000589042.5:c.106112A= (TTN) MANE Select	ENSP00000467141.1:p.Asn35371=
ENST00000591111.5:c.101189A= (TTN)	ENSP00000465570.1:p.Asn33730=
ENST00000615779.4:c.101189A= (TTN)	ENSP00000483597.1:p.Asn33730=
NM_001256850.1:c.101189A= (TTN)	NP_001243779.1:p.Asn33730=
NM_001267550.2:c.106112A= (TTN) MANE Select	NP_001254479.2:p.Asn35371=
NM_003319.4:c.78917A= (TTN)	NP_003310.4:p.Asn26306=
NM_133378.4:c.98408A= (TTN)	NP_596869.4:p.Asn32803=
NM_133432.3:c.79292A= (TTN)	NP_597676.3:p.Asn26431=
NM_133437.4:c.79493A= (TTN)	NP_597681.4:p.Asn26498=
NR_038271.1:n.446+6867T= (TTN-AS1)
NR_038272.1:n.220-5229T= (TTN-AS1)
XM_011511729.1:c.105209A= (TTN)	XP_011510031.1:p.Asn35070=
XM_011511730.1:c.79103A= (TTN)	XP_011510032.1:p.Asn26368=
XM_011511731.1:c.78962A= (TTN)	XP_011510033.1:p.Asn26321=
XM_017004819.1:c.105005A= (TTN)	XP_016860308.1:p.Asn35002=
XM_017004820.1:c.100403A= (TTN)	XP_016860309.1:p.Asn33468=
XM_017004821.1:c.100400A= (TTN)	XP_016860310.1:p.Asn33467=
XM_017004822.1:c.97442A= (TTN)	XP_016860311.1:p.Asn32481=
XM_017004823.1:c.79058A= (TTN)	XP_016860312.1:p.Asn26353=
XM_024453094.1:c.100553A= (TTN)	XP_024308862.1:p.Asn33518=
XM_024453095.1:c.100550A= (TTN)	XP_024308863.1:p.Asn33517=
XM_024453096.1:c.99983A= (TTN)	XP_024308864.1:p.Asn33328=
XM_024453097.1:c.97325A= (TTN)	XP_024308865.1:p.Asn32442=
XM_024453098.1:c.97244A= (TTN)	XP_024308866.1:p.Asn32415=
XM_024453099.1:c.79007A= (TTN)	XP_024308867.1:p.Asn26336=
XM_024453100.1:c.68861A= (TTN)	XP_024308868.1:p.Asn22954=