Canonical Allele Identifier: CA2662125519

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178530183-ATTTAGAAGATAAAATAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530198_178530214del , CM000664.2:g.178530198_178530214del	GRCh38
NC_000002.11:g.179394925_179394941del , CM000664.1:g.179394925_179394941del	GRCh37
NC_000002.10:g.179103171_179103187del	NCBI36
NG_011618.3:g.305603_305619del , LRG_391:g.305603_305619del
NG_051363.1:g.12372_12388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98670+41_98670+57del (TTN)	ENSP00000343764.6:n.98670+41_98670+57del
ENST00000342175.11:c.79755+41_79755+57del (TTN)	ENSP00000340554.6:n.79755+41_79755+57del
ENST00000359218.10:c.79554+41_79554+57del (TTN)	ENSP00000352154.5:n.79554+41_79554+57del
ENST00000342175.10:c.79755+41_79755+57del (TTN)	ENSP00000340554.6:n.79755+41_79755+57del
ENST00000342992.10:c.98670+41_98670+57del (TTN)	ENSP00000343764.6:n.98670+41_98670+57del
ENST00000359218.9:c.79554+41_79554+57del (TTN)	ENSP00000352154.5:n.79554+41_79554+57del
ENST00000460472.6:c.79179+41_79179+57del (TTN)	ENSP00000434586.1:n.79179+41_79179+57del
ENST00000589042.5:c.106374+41_106374+57del (TTN) MANE Select	ENSP00000467141.1:n.106374+41_106374+57del
ENST00000591111.5:c.101451+41_101451+57del (TTN)	ENSP00000465570.1:n.101451+41_101451+57del
ENST00000615779.4:c.101451+41_101451+57del (TTN)	ENSP00000483597.1:n.101451+41_101451+57del
NM_001256850.1:c.101451+41_101451+57del (TTN)	NP_001243779.1:n.101451+41_101451+57del
NM_001267550.2:c.106374+41_106374+57del (TTN) MANE Select	NP_001254479.2:n.106374+41_106374+57del
NM_003319.4:c.79179+41_79179+57del (TTN)	NP_003310.4:n.79179+41_79179+57del
NM_133378.4:c.98670+41_98670+57del (TTN)	NP_596869.4:n.98670+41_98670+57del
NM_133432.3:c.79554+41_79554+57del (TTN)	NP_597676.3:n.79554+41_79554+57del
NM_133437.4:c.79755+41_79755+57del (TTN)	NP_597681.4:n.79755+41_79755+57del
NR_038271.1:n.446+6562_446+6578del (TTN-AS1)
NR_038272.1:n.220-5534_220-5518del (TTN-AS1)
XM_011511729.1:c.105471+41_105471+57del (TTN)	XP_011510031.1:n.105471+41_105471+57del
XM_011511730.1:c.79365+41_79365+57del (TTN)	XP_011510032.1:n.79365+41_79365+57del
XM_011511731.1:c.79224+41_79224+57del (TTN)	XP_011510033.1:n.79224+41_79224+57del
XM_017004819.1:c.105267+41_105267+57del (TTN)	XP_016860308.1:n.105267+41_105267+57del
XM_017004820.1:c.100665+41_100665+57del (TTN)	XP_016860309.1:n.100665+41_100665+57del
XM_017004821.1:c.100662+41_100662+57del (TTN)	XP_016860310.1:n.100662+41_100662+57del
XM_017004822.1:c.97704+41_97704+57del (TTN)	XP_016860311.1:n.97704+41_97704+57del
XM_017004823.1:c.79320+41_79320+57del (TTN)	XP_016860312.1:n.79320+41_79320+57del
XM_024453094.1:c.100815+41_100815+57del (TTN)	XP_024308862.1:n.100815+41_100815+57del
XM_024453095.1:c.100812+41_100812+57del (TTN)	XP_024308863.1:n.100812+41_100812+57del
XM_024453096.1:c.100245+41_100245+57del (TTN)	XP_024308864.1:n.100245+41_100245+57del
XM_024453097.1:c.97587+41_97587+57del (TTN)	XP_024308865.1:n.97587+41_97587+57del
XM_024453098.1:c.97506+41_97506+57del (TTN)	XP_024308866.1:n.97506+41_97506+57del
XM_024453099.1:c.79269+41_79269+57del (TTN)	XP_024308867.1:n.79269+41_79269+57del
XM_024453100.1:c.69123+41_69123+57del (TTN)	XP_024308868.1:n.69123+41_69123+57del