Canonical Allele Identifier: CA1310539820

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591103_178591104delinsTA , CM000664.2:g.178591103_178591104delinsTA	GRCh38
NC_000002.11:g.179455830_179455831delinsTA , CM000664.1:g.179455830_179455831delinsTA	GRCh37
NC_000002.10:g.179164076_179164077delinsTA	NCBI36
NG_011618.3:g.244699_244700delinsTA , LRG_391:g.244699_244700delinsTA
NG_051363.1:g.73277_73278delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52917_52918delinsTA (TTN)	ENSP00000343764.6:p.Tyr17639=
ENST00000342175.11:c.34002_34003delinsTA (TTN)	ENSP00000340554.6:p.Tyr11334=
ENST00000359218.10:c.33801_33802delinsTA (TTN)	ENSP00000352154.5:p.Tyr11267=
ENST00000342175.10:c.34002_34003delinsTA (TTN)	ENSP00000340554.6:p.Tyr11334=
ENST00000342992.10:c.52917_52918delinsTA (TTN)	ENSP00000343764.6:p.Tyr17639=
ENST00000359218.9:c.33801_33802delinsTA (TTN)	ENSP00000352154.5:p.Tyr11267=
ENST00000460472.6:c.33426_33427delinsTA (TTN)	ENSP00000434586.1:p.Tyr11142=
ENST00000589042.5:c.60621_60622delinsTA (TTN) MANE Select	ENSP00000467141.1:p.Tyr20207=
ENST00000591111.5:c.55698_55699delinsTA (TTN)	ENSP00000465570.1:p.Tyr18566=
ENST00000615779.4:c.55698_55699delinsTA (TTN)	ENSP00000483597.1:p.Tyr18566=
NM_001256850.1:c.55698_55699delinsTA (TTN)	NP_001243779.1:p.Tyr18566=
NM_001267550.2:c.60621_60622delinsTA (TTN) MANE Select	NP_001254479.2:p.Tyr20207=
NM_003319.4:c.33426_33427delinsTA (TTN)	NP_003310.4:p.Tyr11142=
NM_133378.4:c.52917_52918delinsTA (TTN)	NP_596869.4:p.Tyr17639=
NM_133432.3:c.33801_33802delinsTA (TTN)	NP_597676.3:p.Tyr11267=
NM_133437.4:c.34002_34003delinsTA (TTN)	NP_597681.4:p.Tyr11334=
NR_038271.1:n.597-6493_597-6492delinsTA (TTN-AS1)
NR_038272.1:n.3189-36_3189-35delinsTA (TTN-AS1)
XM_011511729.1:c.59718_59719delinsTA (TTN)	XP_011510031.1:p.Tyr19906=
XM_011511730.1:c.33612_33613delinsTA (TTN)	XP_011510032.1:p.Tyr11204=
XM_011511731.1:c.33471_33472delinsTA (TTN)	XP_011510033.1:p.Tyr11157=
XM_017004819.1:c.59514_59515delinsTA (TTN)	XP_016860308.1:p.Tyr19838=
XM_017004820.1:c.54912_54913delinsTA (TTN)	XP_016860309.1:p.Tyr18304=
XM_017004821.1:c.54909_54910delinsTA (TTN)	XP_016860310.1:p.Tyr18303=
XM_017004822.1:c.51951_51952delinsTA (TTN)	XP_016860311.1:p.Tyr17317=
XM_017004823.1:c.33567_33568delinsTA (TTN)	XP_016860312.1:p.Tyr11189=
XM_024453094.1:c.55062_55063delinsTA (TTN)	XP_024308862.1:p.Tyr18354=
XM_024453095.1:c.55059_55060delinsTA (TTN)	XP_024308863.1:p.Tyr18353=
XM_024453096.1:c.54492_54493delinsTA (TTN)	XP_024308864.1:p.Tyr18164=
XM_024453097.1:c.51834_51835delinsTA (TTN)	XP_024308865.1:p.Tyr17278=
XM_024453098.1:c.51753_51754delinsTA (TTN)	XP_024308866.1:p.Tyr17251=
XM_024453099.1:c.33516_33517delinsTA (TTN)	XP_024308867.1:p.Tyr11172=
XM_024453100.1:c.23370_23371delinsTA (TTN)	XP_024308868.1:p.Tyr7790=