Canonical Allele Identifier: CA2577198651

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178569880-TTATGTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569885_178569890del , CM000664.2:g.178569885_178569890del	GRCh38
NC_000002.11:g.179434612_179434617del , CM000664.1:g.179434612_179434617del	GRCh37
NC_000002.10:g.179142858_179142863del	NCBI36
NG_011618.3:g.265917_265922del , LRG_391:g.265917_265922del
NG_051363.1:g.52059_52064del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.68542_68547del (TTN)	ENSP00000343764.6:p.Asp22848_Ile22849del
ENST00000342175.11:c.49627_49632del (TTN)	ENSP00000340554.6:p.Asp16543_Ile16544del
ENST00000359218.10:c.49426_49431del (TTN)	ENSP00000352154.5:p.Asp16476_Ile16477del
ENST00000342175.10:c.49627_49632del (TTN)	ENSP00000340554.6:p.Asp16543_Ile16544del
ENST00000342992.10:c.68542_68547del (TTN)	ENSP00000343764.6:p.Asp22848_Ile22849del
ENST00000359218.9:c.49426_49431del (TTN)	ENSP00000352154.5:p.Asp16476_Ile16477del
ENST00000460472.6:c.49051_49056del (TTN)	ENSP00000434586.1:p.Asp16351_Ile16352del
ENST00000589042.5:c.76246_76251del (TTN) MANE Select	ENSP00000467141.1:p.Asp25416_Ile25417del
ENST00000591111.5:c.71323_71328del (TTN)	ENSP00000465570.1:p.Asp23775_Ile23776del
ENST00000615779.4:c.71323_71328del (TTN)	ENSP00000483597.1:p.Asp23775_Ile23776del
NM_001256850.1:c.71323_71328del (TTN)	NP_001243779.1:p.Asp23775_Ile23776del
NM_001267550.2:c.76246_76251del (TTN) MANE Select	NP_001254479.2:p.Asp25416_Ile25417del
NM_003319.4:c.49051_49056del (TTN)	NP_003310.4:p.Asp16351_Ile16352del
NM_133378.4:c.68542_68547del (TTN)	NP_596869.4:p.Asp22848_Ile22849del
NM_133432.3:c.49426_49431del (TTN)	NP_597676.3:p.Asp16476_Ile16477del
NM_133437.4:c.49627_49632del (TTN)	NP_597681.4:p.Asp16543_Ile16544del
NR_038271.1:n.447-1415_447-1410del (TTN-AS1)
NR_038272.1:n.2044-12687_2044-12682del (TTN-AS1)
XM_011511729.1:c.75343_75348del (TTN)	XP_011510031.1:p.Asp25115_Ile25116del
XM_011511730.1:c.49237_49242del (TTN)	XP_011510032.1:p.Asp16413_Ile16414del
XM_011511731.1:c.49096_49101del (TTN)	XP_011510033.1:p.Asp16366_Ile16367del
XM_017004819.1:c.75139_75144del (TTN)	XP_016860308.1:p.Asp25047_Ile25048del
XM_017004820.1:c.70537_70542del (TTN)	XP_016860309.1:p.Asp23513_Ile23514del
XM_017004821.1:c.70534_70539del (TTN)	XP_016860310.1:p.Asp23512_Ile23513del
XM_017004822.1:c.67576_67581del (TTN)	XP_016860311.1:p.Asp22526_Ile22527del
XM_017004823.1:c.49192_49197del (TTN)	XP_016860312.1:p.Asp16398_Ile16399del
XM_024453094.1:c.70687_70692del (TTN)	XP_024308862.1:p.Asp23563_Ile23564del
XM_024453095.1:c.70684_70689del (TTN)	XP_024308863.1:p.Asp23562_Ile23563del
XM_024453096.1:c.70117_70122del (TTN)	XP_024308864.1:p.Asp23373_Ile23374del
XM_024453097.1:c.67459_67464del (TTN)	XP_024308865.1:p.Asp22487_Ile22488del
XM_024453098.1:c.67378_67383del (TTN)	XP_024308866.1:p.Asp22460_Ile22461del
XM_024453099.1:c.49141_49146del (TTN)	XP_024308867.1:p.Asp16381_Ile16382del
XM_024453100.1:c.38995_39000del (TTN)	XP_024308868.1:p.Asp12999_Ile13000del