Canonical Allele Identifier: CA1310537548

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586613_178586614delinsCA , CM000664.2:g.178586613_178586614delinsCA	GRCh38
NC_000002.11:g.179451340_179451341delinsCA , CM000664.1:g.179451340_179451341delinsCA	GRCh37
NC_000002.10:g.179159586_179159587delinsCA	NCBI36
NG_011618.3:g.249189_249190delinsTG , LRG_391:g.249189_249190delinsTG
NG_051363.1:g.68787_68788delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.56583_56584delinsTG (TTN)	ENSP00000343764.6:p.Thr18861=
ENST00000342175.11:c.37668_37669delinsTG (TTN)	ENSP00000340554.6:p.Thr12556=
ENST00000359218.10:c.37467_37468delinsTG (TTN)	ENSP00000352154.5:p.Thr12489=
ENST00000342175.10:c.37668_37669delinsTG (TTN)	ENSP00000340554.6:p.Thr12556=
ENST00000342992.10:c.56583_56584delinsTG (TTN)	ENSP00000343764.6:p.Thr18861=
ENST00000359218.9:c.37467_37468delinsTG (TTN)	ENSP00000352154.5:p.Thr12489=
ENST00000460472.6:c.37092_37093delinsTG (TTN)	ENSP00000434586.1:p.Thr12364=
ENST00000589042.5:c.64287_64288delinsTG (TTN) MANE Select	ENSP00000467141.1:p.Thr21429=
ENST00000591111.5:c.59364_59365delinsTG (TTN)	ENSP00000465570.1:p.Thr19788=
ENST00000615779.4:c.59364_59365delinsTG (TTN)	ENSP00000483597.1:p.Thr19788=
NM_001256850.1:c.59364_59365delinsTG (TTN)	NP_001243779.1:p.Thr19788=
NM_001267550.2:c.64287_64288delinsTG (TTN) MANE Select	NP_001254479.2:p.Thr21429=
NM_003319.4:c.37092_37093delinsTG (TTN)	NP_003310.4:p.Thr12364=
NM_133378.4:c.56583_56584delinsTG (TTN)	NP_596869.4:p.Thr18861=
NM_133432.3:c.37467_37468delinsTG (TTN)	NP_597676.3:p.Thr12489=
NM_133437.4:c.37668_37669delinsTG (TTN)	NP_597681.4:p.Thr12556=
NR_038271.1:n.597-10983_597-10982delinsCA (TTN-AS1)
NR_038272.1:n.3188+1620_3188+1621delinsCA (TTN-AS1)
XM_011511729.1:c.63384_63385delinsTG (TTN)	XP_011510031.1:p.Thr21128=
XM_011511730.1:c.37278_37279delinsTG (TTN)	XP_011510032.1:p.Thr12426=
XM_011511731.1:c.37137_37138delinsTG (TTN)	XP_011510033.1:p.Thr12379=
XM_017004819.1:c.63180_63181delinsTG (TTN)	XP_016860308.1:p.Thr21060=
XM_017004820.1:c.58578_58579delinsTG (TTN)	XP_016860309.1:p.Thr19526=
XM_017004821.1:c.58575_58576delinsTG (TTN)	XP_016860310.1:p.Thr19525=
XM_017004822.1:c.55617_55618delinsTG (TTN)	XP_016860311.1:p.Thr18539=
XM_017004823.1:c.37233_37234delinsTG (TTN)	XP_016860312.1:p.Thr12411=
XM_024453094.1:c.58728_58729delinsTG (TTN)	XP_024308862.1:p.Thr19576=
XM_024453095.1:c.58725_58726delinsTG (TTN)	XP_024308863.1:p.Thr19575=
XM_024453096.1:c.58158_58159delinsTG (TTN)	XP_024308864.1:p.Thr19386=
XM_024453097.1:c.55500_55501delinsTG (TTN)	XP_024308865.1:p.Thr18500=
XM_024453098.1:c.55419_55420delinsTG (TTN)	XP_024308866.1:p.Thr18473=
XM_024453099.1:c.37182_37183delinsTG (TTN)	XP_024308867.1:p.Thr12394=
XM_024453100.1:c.27036_27037delinsTG (TTN)	XP_024308868.1:p.Thr9012=