Canonical Allele Identifier: CA2662130854

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178591961-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591965_178591966del , CM000664.2:g.178591965_178591966del	GRCh38
NC_000002.11:g.179456692_179456693del , CM000664.1:g.179456692_179456693del	GRCh37
NC_000002.10:g.179164938_179164939del	NCBI36
NG_011618.3:g.243840_243841del , LRG_391:g.243840_243841del
NG_051363.1:g.74139_74140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52222+15_52222+16del (TTN)	ENSP00000343764.6:n.52222+15_52222+16del
ENST00000342175.11:c.33307+15_33307+16del (TTN)	ENSP00000340554.6:n.33307+15_33307+16del
ENST00000359218.10:c.33106+15_33106+16del (TTN)	ENSP00000352154.5:n.33106+15_33106+16del
ENST00000342175.10:c.33307+15_33307+16del (TTN)	ENSP00000340554.6:n.33307+15_33307+16del
ENST00000342992.10:c.52222+15_52222+16del (TTN)	ENSP00000343764.6:n.52222+15_52222+16del
ENST00000359218.9:c.33106+15_33106+16del (TTN)	ENSP00000352154.5:n.33106+15_33106+16del
ENST00000460472.6:c.32731+15_32731+16del (TTN)	ENSP00000434586.1:n.32731+15_32731+16del
ENST00000589042.5:c.59926+15_59926+16del (TTN) MANE Select	ENSP00000467141.1:n.59926+15_59926+16del
ENST00000591111.5:c.55003+15_55003+16del (TTN)	ENSP00000465570.1:n.55003+15_55003+16del
ENST00000615779.4:c.55003+15_55003+16del (TTN)	ENSP00000483597.1:n.55003+15_55003+16del
NM_001256850.1:c.55003+15_55003+16del (TTN)	NP_001243779.1:n.55003+15_55003+16del
NM_001267550.2:c.59926+15_59926+16del (TTN) MANE Select	NP_001254479.2:n.59926+15_59926+16del
NM_003319.4:c.32731+15_32731+16del (TTN)	NP_003310.4:n.32731+15_32731+16del
NM_133378.4:c.52222+15_52222+16del (TTN)	NP_596869.4:n.52222+15_52222+16del
NM_133432.3:c.33106+15_33106+16del (TTN)	NP_597676.3:n.33106+15_33106+16del
NM_133437.4:c.33307+15_33307+16del (TTN)	NP_597681.4:n.33307+15_33307+16del
NR_038271.1:n.597-5631_597-5630del (TTN-AS1)
NR_038272.1:n.3364+651_3364+652del (TTN-AS1)
XM_011511729.1:c.59023+15_59023+16del (TTN)	XP_011510031.1:n.59023+15_59023+16del
XM_011511730.1:c.32917+15_32917+16del (TTN)	XP_011510032.1:n.32917+15_32917+16del
XM_011511731.1:c.32776+15_32776+16del (TTN)	XP_011510033.1:n.32776+15_32776+16del
XM_017004819.1:c.58819+15_58819+16del (TTN)	XP_016860308.1:n.58819+15_58819+16del
XM_017004820.1:c.54217+15_54217+16del (TTN)	XP_016860309.1:n.54217+15_54217+16del
XM_017004821.1:c.54214+15_54214+16del (TTN)	XP_016860310.1:n.54214+15_54214+16del
XM_017004822.1:c.51256+15_51256+16del (TTN)	XP_016860311.1:n.51256+15_51256+16del
XM_017004823.1:c.32872+15_32872+16del (TTN)	XP_016860312.1:n.32872+15_32872+16del
XM_024453094.1:c.54367+15_54367+16del (TTN)	XP_024308862.1:n.54367+15_54367+16del
XM_024453095.1:c.54364+15_54364+16del (TTN)	XP_024308863.1:n.54364+15_54364+16del
XM_024453096.1:c.53797+15_53797+16del (TTN)	XP_024308864.1:n.53797+15_53797+16del
XM_024453097.1:c.51139+15_51139+16del (TTN)	XP_024308865.1:n.51139+15_51139+16del
XM_024453098.1:c.51058+15_51058+16del (TTN)	XP_024308866.1:n.51058+15_51058+16del
XM_024453099.1:c.32821+15_32821+16del (TTN)	XP_024308867.1:n.32821+15_32821+16del
XM_024453100.1:c.22675+15_22675+16del (TTN)	XP_024308868.1:n.22675+15_22675+16del