Canonical Allele Identifier: CA1310514295

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527090_178527096delinsACCATCT , CM000664.2:g.178527090_178527096delinsACCATCT	GRCh38
NC_000002.11:g.179391817_179391823delinsACCATCT , CM000664.1:g.179391817_179391823delinsACCATCT	GRCh37
NC_000002.10:g.179100063_179100069delinsACCATCT	NCBI36
NG_011618.3:g.308707_308713delinsAGATGGT , LRG_391:g.308707_308713delinsAGATGGT
NG_051363.1:g.9264_9270delinsACCATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100188_100194delinsAGATGGT (TTN)	ENSP00000343764.6:p.Gln33396=
ENST00000342175.11:c.81273_81279delinsAGATGGT (TTN)	ENSP00000340554.6:p.Gln27091=
ENST00000359218.10:c.81072_81078delinsAGATGGT (TTN)	ENSP00000352154.5:p.Gln27024=
ENST00000342175.10:c.81273_81279delinsAGATGGT (TTN)	ENSP00000340554.6:p.Gln27091=
ENST00000342992.10:c.100188_100194delinsAGATGGT (TTN)	ENSP00000343764.6:p.Gln33396=
ENST00000359218.9:c.81072_81078delinsAGATGGT (TTN)	ENSP00000352154.5:p.Gln27024=
ENST00000460472.6:c.80697_80703delinsAGATGGT (TTN)	ENSP00000434586.1:p.Gln26899=
ENST00000589042.5:c.107892_107898delinsAGATGGT (TTN) MANE Select	ENSP00000467141.1:p.Gln35964=
ENST00000591111.5:c.102969_102975delinsAGATGGT (TTN)	ENSP00000465570.1:p.Gln34323=
ENST00000615779.4:c.102969_102975delinsAGATGGT (TTN)	ENSP00000483597.1:p.Gln34323=
NM_001256850.1:c.102969_102975delinsAGATGGT (TTN)	NP_001243779.1:p.Gln34323=
NM_001267550.2:c.107892_107898delinsAGATGGT (TTN) MANE Select	NP_001254479.2:p.Gln35964=
NM_003319.4:c.80697_80703delinsAGATGGT (TTN)	NP_003310.4:p.Gln26899=
NM_133378.4:c.100188_100194delinsAGATGGT (TTN)	NP_596869.4:p.Gln33396=
NM_133432.3:c.81072_81078delinsAGATGGT (TTN)	NP_597676.3:p.Gln27024=
NM_133437.4:c.81273_81279delinsAGATGGT (TTN)	NP_597681.4:p.Gln27091=
NR_038271.1:n.446+3454_446+3460delinsACCATCT (TTN-AS1)
NR_038272.1:n.219+3454_219+3460delinsACCATCT (TTN-AS1)
XM_011511729.1:c.106989_106995delinsAGATGGT (TTN)	XP_011510031.1:p.Gln35663=
XM_011511730.1:c.80883_80889delinsAGATGGT (TTN)	XP_011510032.1:p.Gln26961=
XM_011511731.1:c.80742_80748delinsAGATGGT (TTN)	XP_011510033.1:p.Gln26914=
XM_017004819.1:c.106785_106791delinsAGATGGT (TTN)	XP_016860308.1:p.Gln35595=
XM_017004820.1:c.102183_102189delinsAGATGGT (TTN)	XP_016860309.1:p.Gln34061=
XM_017004821.1:c.102180_102186delinsAGATGGT (TTN)	XP_016860310.1:p.Gln34060=
XM_017004822.1:c.99222_99228delinsAGATGGT (TTN)	XP_016860311.1:p.Gln33074=
XM_017004823.1:c.80838_80844delinsAGATGGT (TTN)	XP_016860312.1:p.Gln26946=
XM_024453094.1:c.102333_102339delinsAGATGGT (TTN)	XP_024308862.1:p.Gln34111=
XM_024453095.1:c.102330_102336delinsAGATGGT (TTN)	XP_024308863.1:p.Gln34110=
XM_024453096.1:c.101763_101769delinsAGATGGT (TTN)	XP_024308864.1:p.Gln33921=
XM_024453097.1:c.99105_99111delinsAGATGGT (TTN)	XP_024308865.1:p.Gln33035=
XM_024453098.1:c.99024_99030delinsAGATGGT (TTN)	XP_024308866.1:p.Gln33008=
XM_024453099.1:c.80787_80793delinsAGATGGT (TTN)	XP_024308867.1:p.Gln26929=
XM_024453100.1:c.70641_70647delinsAGATGGT (TTN)	XP_024308868.1:p.Gln23547=