Canonical Allele Identifier: CA2586970729

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530088_178530089del , CM000664.2:g.178530088_178530089del	GRCh38
NC_000002.11:g.179394815_179394816del , CM000664.1:g.179394815_179394816del	GRCh37
NC_000002.10:g.179103061_179103062del	NCBI36
NG_011618.3:g.305718_305719del , LRG_391:g.305718_305719del
NG_051363.1:g.12262_12263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98702_98703del (TTN)	ENSP00000343764.6:p.Ser32901Ter
ENST00000342175.11:c.79787_79788del (TTN)	ENSP00000340554.6:p.Ser26596Ter
ENST00000359218.10:c.79586_79587del (TTN)	ENSP00000352154.5:p.Ser26529Ter
ENST00000342175.10:c.79787_79788del (TTN)	ENSP00000340554.6:p.Ser26596Ter
ENST00000342992.10:c.98702_98703del (TTN)	ENSP00000343764.6:p.Ser32901Ter
ENST00000359218.9:c.79586_79587del (TTN)	ENSP00000352154.5:p.Ser26529Ter
ENST00000460472.6:c.79211_79212del (TTN)	ENSP00000434586.1:p.Ser26404Ter
ENST00000589042.5:c.106406_106407del (TTN) MANE Select	ENSP00000467141.1:p.Ser35469Ter
ENST00000591111.5:c.101483_101484del (TTN)	ENSP00000465570.1:p.Ser33828Ter
ENST00000615779.4:c.101483_101484del (TTN)	ENSP00000483597.1:p.Ser33828Ter
NM_001256850.1:c.101483_101484del (TTN)	NP_001243779.1:p.Ser33828Ter
NM_001267550.2:c.106406_106407del (TTN) MANE Select	NP_001254479.2:p.Ser35469Ter
NM_003319.4:c.79211_79212del (TTN)	NP_003310.4:p.Ser26404Ter
NM_133378.4:c.98702_98703del (TTN)	NP_596869.4:p.Ser32901Ter
NM_133432.3:c.79586_79587del (TTN)	NP_597676.3:p.Ser26529Ter
NM_133437.4:c.79787_79788del (TTN)	NP_597681.4:p.Ser26596Ter
NR_038271.1:n.446+6452_446+6453del (TTN-AS1)
NR_038272.1:n.220-5644_220-5643del (TTN-AS1)
XM_011511729.1:c.105503_105504del (TTN)	XP_011510031.1:p.Ser35168Ter
XM_011511730.1:c.79397_79398del (TTN)	XP_011510032.1:p.Ser26466Ter
XM_011511731.1:c.79256_79257del (TTN)	XP_011510033.1:p.Ser26419Ter
XM_017004819.1:c.105299_105300del (TTN)	XP_016860308.1:p.Ser35100Ter
XM_017004820.1:c.100697_100698del (TTN)	XP_016860309.1:p.Ser33566Ter
XM_017004821.1:c.100694_100695del (TTN)	XP_016860310.1:p.Ser33565Ter
XM_017004822.1:c.97736_97737del (TTN)	XP_016860311.1:p.Ser32579Ter
XM_017004823.1:c.79352_79353del (TTN)	XP_016860312.1:p.Ser26451Ter
XM_024453094.1:c.100847_100848del (TTN)	XP_024308862.1:p.Ser33616Ter
XM_024453095.1:c.100844_100845del (TTN)	XP_024308863.1:p.Ser33615Ter
XM_024453096.1:c.100277_100278del (TTN)	XP_024308864.1:p.Ser33426Ter
XM_024453097.1:c.97619_97620del (TTN)	XP_024308865.1:p.Ser32540Ter
XM_024453098.1:c.97538_97539del (TTN)	XP_024308866.1:p.Ser32513Ter
XM_024453099.1:c.79301_79302del (TTN)	XP_024308867.1:p.Ser26434Ter
XM_024453100.1:c.69155_69156del (TTN)	XP_024308868.1:p.Ser23052Ter