Canonical Allele Identifier: CA1310524219

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547739_178547745delinsACACCAG , CM000664.2:g.178547739_178547745delinsACACCAG	GRCh38
NC_000002.11:g.179412466_179412472delinsACACCAG , CM000664.1:g.179412466_179412472delinsACACCAG	GRCh37
NC_000002.10:g.179120712_179120718delinsACACCAG	NCBI36
NG_011618.3:g.288058_288064delinsCTGGTGT , LRG_391:g.288058_288064delinsCTGGTGT
NG_051363.1:g.29913_29919delinsACACCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86177_86183delinsCTGGTGT (TTN)	ENSP00000343764.6:p.Ala28726=
ENST00000342175.11:c.67262_67268delinsCTGGTGT (TTN)	ENSP00000340554.6:p.Ala22421=
ENST00000359218.10:c.67061_67067delinsCTGGTGT (TTN)	ENSP00000352154.5:p.Ala22354=
ENST00000342175.10:c.67262_67268delinsCTGGTGT (TTN)	ENSP00000340554.6:p.Ala22421=
ENST00000342992.10:c.86177_86183delinsCTGGTGT (TTN)	ENSP00000343764.6:p.Ala28726=
ENST00000359218.9:c.67061_67067delinsCTGGTGT (TTN)	ENSP00000352154.5:p.Ala22354=
ENST00000460472.6:c.66686_66692delinsCTGGTGT (TTN)	ENSP00000434586.1:p.Ala22229=
ENST00000589042.5:c.93881_93887delinsCTGGTGT (TTN) MANE Select	ENSP00000467141.1:p.Ala31294=
ENST00000591111.5:c.88958_88964delinsCTGGTGT (TTN)	ENSP00000465570.1:p.Ala29653=
ENST00000615779.4:c.88958_88964delinsCTGGTGT (TTN)	ENSP00000483597.1:p.Ala29653=
NM_001256850.1:c.88958_88964delinsCTGGTGT (TTN)	NP_001243779.1:p.Ala29653=
NM_001267550.2:c.93881_93887delinsCTGGTGT (TTN) MANE Select	NP_001254479.2:p.Ala31294=
NM_003319.4:c.66686_66692delinsCTGGTGT (TTN)	NP_003310.4:p.Ala22229=
NM_133378.4:c.86177_86183delinsCTGGTGT (TTN)	NP_596869.4:p.Ala28726=
NM_133432.3:c.67061_67067delinsCTGGTGT (TTN)	NP_597676.3:p.Ala22354=
NM_133437.4:c.67262_67268delinsCTGGTGT (TTN)	NP_597681.4:p.Ala22421=
NR_038271.1:n.447-23561_447-23555delinsACACCAG (TTN-AS1)
NR_038272.1:n.2043+5378_2043+5384delinsACACCAG (TTN-AS1)
XM_011511729.1:c.92978_92984delinsCTGGTGT (TTN)	XP_011510031.1:p.Ala30993=
XM_011511730.1:c.66872_66878delinsCTGGTGT (TTN)	XP_011510032.1:p.Ala22291=
XM_011511731.1:c.66731_66737delinsCTGGTGT (TTN)	XP_011510033.1:p.Ala22244=
XM_017004819.1:c.92774_92780delinsCTGGTGT (TTN)	XP_016860308.1:p.Ala30925=
XM_017004820.1:c.88172_88178delinsCTGGTGT (TTN)	XP_016860309.1:p.Ala29391=
XM_017004821.1:c.88169_88175delinsCTGGTGT (TTN)	XP_016860310.1:p.Ala29390=
XM_017004822.1:c.85211_85217delinsCTGGTGT (TTN)	XP_016860311.1:p.Ala28404=
XM_017004823.1:c.66827_66833delinsCTGGTGT (TTN)	XP_016860312.1:p.Ala22276=
XM_024453094.1:c.88322_88328delinsCTGGTGT (TTN)	XP_024308862.1:p.Ala29441=
XM_024453095.1:c.88319_88325delinsCTGGTGT (TTN)	XP_024308863.1:p.Ala29440=
XM_024453096.1:c.87752_87758delinsCTGGTGT (TTN)	XP_024308864.1:p.Ala29251=
XM_024453097.1:c.85094_85100delinsCTGGTGT (TTN)	XP_024308865.1:p.Ala28365=
XM_024453098.1:c.85013_85019delinsCTGGTGT (TTN)	XP_024308866.1:p.Ala28338=
XM_024453099.1:c.66776_66782delinsCTGGTGT (TTN)	XP_024308867.1:p.Ala22259=
XM_024453100.1:c.56630_56636delinsCTGGTGT (TTN)	XP_024308868.1:p.Ala18877=