Canonical Allele Identifier: CA2586965396

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591107del , CM000664.2:g.178591107del	GRCh38
NC_000002.11:g.179455834del , CM000664.1:g.179455834del	GRCh37
NC_000002.10:g.179164080del	NCBI36
NG_011618.3:g.244697del , LRG_391:g.244697del
NG_051363.1:g.73281del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52915del (TTN)	ENSP00000343764.6:p.Tyr17639IlefsTer25
ENST00000342175.11:c.34000del (TTN)	ENSP00000340554.6:p.Tyr11334IlefsTer25
ENST00000359218.10:c.33799del (TTN)	ENSP00000352154.5:p.Tyr11267IlefsTer25
ENST00000342175.10:c.34000del (TTN)	ENSP00000340554.6:p.Tyr11334IlefsTer25
ENST00000342992.10:c.52915del (TTN)	ENSP00000343764.6:p.Tyr17639IlefsTer25
ENST00000359218.9:c.33799del (TTN)	ENSP00000352154.5:p.Tyr11267IlefsTer25
ENST00000460472.6:c.33424del (TTN)	ENSP00000434586.1:p.Tyr11142IlefsTer25
ENST00000589042.5:c.60619del (TTN) MANE Select	ENSP00000467141.1:p.Tyr20207IlefsTer25
ENST00000591111.5:c.55696del (TTN)	ENSP00000465570.1:p.Tyr18566IlefsTer25
ENST00000615779.4:c.55696del (TTN)	ENSP00000483597.1:p.Tyr18566IlefsTer25
NM_001256850.1:c.55696del (TTN)	NP_001243779.1:p.Tyr18566IlefsTer25
NM_001267550.2:c.60619del (TTN) MANE Select	NP_001254479.2:p.Tyr20207IlefsTer25
NM_003319.4:c.33424del (TTN)	NP_003310.4:p.Tyr11142IlefsTer25
NM_133378.4:c.52915del (TTN)	NP_596869.4:p.Tyr17639IlefsTer25
NM_133432.3:c.33799del (TTN)	NP_597676.3:p.Tyr11267IlefsTer25
NM_133437.4:c.34000del (TTN)	NP_597681.4:p.Tyr11334IlefsTer25
NR_038271.1:n.597-6489del (TTN-AS1)
NR_038272.1:n.3189-32del (TTN-AS1)
XM_011511729.1:c.59716del (TTN)	XP_011510031.1:p.Tyr19906IlefsTer25
XM_011511730.1:c.33610del (TTN)	XP_011510032.1:p.Tyr11204IlefsTer25
XM_011511731.1:c.33469del (TTN)	XP_011510033.1:p.Tyr11157IlefsTer25
XM_017004819.1:c.59512del (TTN)	XP_016860308.1:p.Tyr19838IlefsTer25
XM_017004820.1:c.54910del (TTN)	XP_016860309.1:p.Tyr18304IlefsTer25
XM_017004821.1:c.54907del (TTN)	XP_016860310.1:p.Tyr18303IlefsTer25
XM_017004822.1:c.51949del (TTN)	XP_016860311.1:p.Tyr17317IlefsTer25
XM_017004823.1:c.33565del (TTN)	XP_016860312.1:p.Tyr11189IlefsTer25
XM_024453094.1:c.55060del (TTN)	XP_024308862.1:p.Tyr18354IlefsTer25
XM_024453095.1:c.55057del (TTN)	XP_024308863.1:p.Tyr18353IlefsTer25
XM_024453096.1:c.54490del (TTN)	XP_024308864.1:p.Tyr18164IlefsTer25
XM_024453097.1:c.51832del (TTN)	XP_024308865.1:p.Tyr17278IlefsTer25
XM_024453098.1:c.51751del (TTN)	XP_024308866.1:p.Tyr17251IlefsTer25
XM_024453099.1:c.33514del (TTN)	XP_024308867.1:p.Tyr11172IlefsTer25
XM_024453100.1:c.23368del (TTN)	XP_024308868.1:p.Tyr7790IlefsTer25