Canonical Allele Identifier: CA2662121647

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178527132-G-GTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527135_178527137dup , CM000664.2:g.178527135_178527137dup	GRCh38
NC_000002.11:g.179391862_179391864dup , CM000664.1:g.179391862_179391864dup	GRCh37
NC_000002.10:g.179100108_179100110dup	NCBI36
NG_011618.3:g.308668_308670dup , LRG_391:g.308668_308670dup
NG_051363.1:g.9309_9311dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100149_100151dup (TTN)	ENSP00000343764.6:p.Asp33384_Leu33385insAsp
ENST00000342175.11:c.81234_81236dup (TTN)	ENSP00000340554.6:p.Asp27079_Leu27080insAsp
ENST00000359218.10:c.81033_81035dup (TTN)	ENSP00000352154.5:p.Asp27012_Leu27013insAsp
ENST00000342175.10:c.81234_81236dup (TTN)	ENSP00000340554.6:p.Asp27079_Leu27080insAsp
ENST00000342992.10:c.100149_100151dup (TTN)	ENSP00000343764.6:p.Asp33384_Leu33385insAsp
ENST00000359218.9:c.81033_81035dup (TTN)	ENSP00000352154.5:p.Asp27012_Leu27013insAsp
ENST00000460472.6:c.80658_80660dup (TTN)	ENSP00000434586.1:p.Asp26887_Leu26888insAsp
ENST00000589042.5:c.107853_107855dup (TTN) MANE Select	ENSP00000467141.1:p.Asp35952_Leu35953insAsp
ENST00000591111.5:c.102930_102932dup (TTN)	ENSP00000465570.1:p.Asp34311_Leu34312insAsp
ENST00000615779.4:c.102930_102932dup (TTN)	ENSP00000483597.1:p.Asp34311_Leu34312insAsp
NM_001256850.1:c.102930_102932dup (TTN)	NP_001243779.1:p.Asp34311_Leu34312insAsp
NM_001267550.2:c.107853_107855dup (TTN) MANE Select	NP_001254479.2:p.Asp35952_Leu35953insAsp
NM_003319.4:c.80658_80660dup (TTN)	NP_003310.4:p.Asp26887_Leu26888insAsp
NM_133378.4:c.100149_100151dup (TTN)	NP_596869.4:p.Asp33384_Leu33385insAsp
NM_133432.3:c.81033_81035dup (TTN)	NP_597676.3:p.Asp27012_Leu27013insAsp
NM_133437.4:c.81234_81236dup (TTN)	NP_597681.4:p.Asp27079_Leu27080insAsp
NR_038271.1:n.446+3499_446+3501dup (TTN-AS1)
NR_038272.1:n.219+3499_219+3501dup (TTN-AS1)
XM_011511729.1:c.106950_106952dup (TTN)	XP_011510031.1:p.Asp35651_Leu35652insAsp
XM_011511730.1:c.80844_80846dup (TTN)	XP_011510032.1:p.Asp26949_Leu26950insAsp
XM_011511731.1:c.80703_80705dup (TTN)	XP_011510033.1:p.Asp26902_Leu26903insAsp
XM_017004819.1:c.106746_106748dup (TTN)	XP_016860308.1:p.Asp35583_Leu35584insAsp
XM_017004820.1:c.102144_102146dup (TTN)	XP_016860309.1:p.Asp34049_Leu34050insAsp
XM_017004821.1:c.102141_102143dup (TTN)	XP_016860310.1:p.Asp34048_Leu34049insAsp
XM_017004822.1:c.99183_99185dup (TTN)	XP_016860311.1:p.Asp33062_Leu33063insAsp
XM_017004823.1:c.80799_80801dup (TTN)	XP_016860312.1:p.Asp26934_Leu26935insAsp
XM_024453094.1:c.102294_102296dup (TTN)	XP_024308862.1:p.Asp34099_Leu34100insAsp
XM_024453095.1:c.102291_102293dup (TTN)	XP_024308863.1:p.Asp34098_Leu34099insAsp
XM_024453096.1:c.101724_101726dup (TTN)	XP_024308864.1:p.Asp33909_Leu33910insAsp
XM_024453097.1:c.99066_99068dup (TTN)	XP_024308865.1:p.Asp33023_Leu33024insAsp
XM_024453098.1:c.98985_98987dup (TTN)	XP_024308866.1:p.Asp32996_Leu32997insAsp
XM_024453099.1:c.80748_80750dup (TTN)	XP_024308867.1:p.Asp26917_Leu26918insAsp
XM_024453100.1:c.70602_70604dup (TTN)	XP_024308868.1:p.Asp23535_Leu23536insAsp