Canonical Allele Identifier: CA2662129638

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178579402-TAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178579405_178579407del , CM000664.2:g.178579405_178579407del	GRCh38
NC_000002.11:g.179444132_179444134del , CM000664.1:g.179444132_179444134del	GRCh37
NC_000002.10:g.179152378_179152380del	NCBI36
NG_011618.3:g.256398_256400del , LRG_391:g.256398_256400del
NG_051363.1:g.61579_61581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.59933-12_59933-10del (TTN)	ENSP00000343764.6:n.59933-12_59933-10del
ENST00000342175.11:c.41018-12_41018-10del (TTN)	ENSP00000340554.6:n.41018-12_41018-10del
ENST00000359218.10:c.40817-12_40817-10del (TTN)	ENSP00000352154.5:n.40817-12_40817-10del
ENST00000342175.10:c.41018-12_41018-10del (TTN)	ENSP00000340554.6:n.41018-12_41018-10del
ENST00000342992.10:c.59933-12_59933-10del (TTN)	ENSP00000343764.6:n.59933-12_59933-10del
ENST00000359218.9:c.40817-12_40817-10del (TTN)	ENSP00000352154.5:n.40817-12_40817-10del
ENST00000460472.6:c.40442-12_40442-10del (TTN)	ENSP00000434586.1:n.40442-12_40442-10del
ENST00000589042.5:c.67637-12_67637-10del (TTN) MANE Select	ENSP00000467141.1:n.67637-12_67637-10del
ENST00000591111.5:c.62714-12_62714-10del (TTN)	ENSP00000465570.1:n.62714-12_62714-10del
ENST00000615779.4:c.62714-12_62714-10del (TTN)	ENSP00000483597.1:n.62714-12_62714-10del
NM_001256850.1:c.62714-12_62714-10del (TTN)	NP_001243779.1:n.62714-12_62714-10del
NM_001267550.2:c.67637-12_67637-10del (TTN) MANE Select	NP_001254479.2:n.67637-12_67637-10del
NM_003319.4:c.40442-12_40442-10del (TTN)	NP_003310.4:n.40442-12_40442-10del
NM_133378.4:c.59933-12_59933-10del (TTN)	NP_596869.4:n.59933-12_59933-10del
NM_133432.3:c.40817-12_40817-10del (TTN)	NP_597676.3:n.40817-12_40817-10del
NM_133437.4:c.41018-12_41018-10del (TTN)	NP_597681.4:n.41018-12_41018-10del
NR_038271.1:n.596+7956_596+7958del (TTN-AS1)
NR_038272.1:n.2044-3167_2044-3165del (TTN-AS1)
XM_011511729.1:c.66734-12_66734-10del (TTN)	XP_011510031.1:n.66734-12_66734-10del
XM_011511730.1:c.40628-12_40628-10del (TTN)	XP_011510032.1:n.40628-12_40628-10del
XM_011511731.1:c.40487-12_40487-10del (TTN)	XP_011510033.1:n.40487-12_40487-10del
XM_017004819.1:c.66530-12_66530-10del (TTN)	XP_016860308.1:n.66530-12_66530-10del
XM_017004820.1:c.61928-12_61928-10del (TTN)	XP_016860309.1:n.61928-12_61928-10del
XM_017004821.1:c.61925-12_61925-10del (TTN)	XP_016860310.1:n.61925-12_61925-10del
XM_017004822.1:c.58967-12_58967-10del (TTN)	XP_016860311.1:n.58967-12_58967-10del
XM_017004823.1:c.40583-12_40583-10del (TTN)	XP_016860312.1:n.40583-12_40583-10del
XM_024453094.1:c.62078-12_62078-10del (TTN)	XP_024308862.1:n.62078-12_62078-10del
XM_024453095.1:c.62075-12_62075-10del (TTN)	XP_024308863.1:n.62075-12_62075-10del
XM_024453096.1:c.61508-12_61508-10del (TTN)	XP_024308864.1:n.61508-12_61508-10del
XM_024453097.1:c.58850-12_58850-10del (TTN)	XP_024308865.1:n.58850-12_58850-10del
XM_024453098.1:c.58769-12_58769-10del (TTN)	XP_024308866.1:n.58769-12_58769-10del
XM_024453099.1:c.40532-12_40532-10del (TTN)	XP_024308867.1:n.40532-12_40532-10del
XM_024453100.1:c.30386-12_30386-10del (TTN)	XP_024308868.1:n.30386-12_30386-10del