Canonical Allele Identifier: CA1310511460

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1688389077

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530085_178530087del , CM000664.2:g.178530085_178530087del	GRCh38
NC_000002.11:g.179394812_179394814del , CM000664.1:g.179394812_179394814del	GRCh37
NC_000002.10:g.179103058_179103060del	NCBI36
NG_011618.3:g.305716_305718del , LRG_391:g.305716_305718del
NG_051363.1:g.12259_12261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98700_98702del (TTN)	ENSP00000343764.6:p.Ser32901del
ENST00000342175.11:c.79785_79787del (TTN)	ENSP00000340554.6:p.Ser26596del
ENST00000359218.10:c.79584_79586del (TTN)	ENSP00000352154.5:p.Ser26529del
ENST00000342175.10:c.79785_79787del (TTN)	ENSP00000340554.6:p.Ser26596del
ENST00000342992.10:c.98700_98702del (TTN)	ENSP00000343764.6:p.Ser32901del
ENST00000359218.9:c.79584_79586del (TTN)	ENSP00000352154.5:p.Ser26529del
ENST00000460472.6:c.79209_79211del (TTN)	ENSP00000434586.1:p.Ser26404del
ENST00000589042.5:c.106404_106406del (TTN) MANE Select	ENSP00000467141.1:p.Ser35469del
ENST00000591111.5:c.101481_101483del (TTN)	ENSP00000465570.1:p.Ser33828del
ENST00000615779.4:c.101481_101483del (TTN)	ENSP00000483597.1:p.Ser33828del
NM_001256850.1:c.101481_101483del (TTN)	NP_001243779.1:p.Ser33828del
NM_001267550.2:c.106404_106406del (TTN) MANE Select	NP_001254479.2:p.Ser35469del
NM_003319.4:c.79209_79211del (TTN)	NP_003310.4:p.Ser26404del
NM_133378.4:c.98700_98702del (TTN)	NP_596869.4:p.Ser32901del
NM_133432.3:c.79584_79586del (TTN)	NP_597676.3:p.Ser26529del
NM_133437.4:c.79785_79787del (TTN)	NP_597681.4:p.Ser26596del
NR_038271.1:n.446+6449_446+6451del (TTN-AS1)
NR_038272.1:n.220-5647_220-5645del (TTN-AS1)
XM_011511729.1:c.105501_105503del (TTN)	XP_011510031.1:p.Ser35168del
XM_011511730.1:c.79395_79397del (TTN)	XP_011510032.1:p.Ser26466del
XM_011511731.1:c.79254_79256del (TTN)	XP_011510033.1:p.Ser26419del
XM_017004819.1:c.105297_105299del (TTN)	XP_016860308.1:p.Ser35100del
XM_017004820.1:c.100695_100697del (TTN)	XP_016860309.1:p.Ser33566del
XM_017004821.1:c.100692_100694del (TTN)	XP_016860310.1:p.Ser33565del
XM_017004822.1:c.97734_97736del (TTN)	XP_016860311.1:p.Ser32579del
XM_017004823.1:c.79350_79352del (TTN)	XP_016860312.1:p.Ser26451del
XM_024453094.1:c.100845_100847del (TTN)	XP_024308862.1:p.Ser33616del
XM_024453095.1:c.100842_100844del (TTN)	XP_024308863.1:p.Ser33615del
XM_024453096.1:c.100275_100277del (TTN)	XP_024308864.1:p.Ser33426del
XM_024453097.1:c.97617_97619del (TTN)	XP_024308865.1:p.Ser32540del
XM_024453098.1:c.97536_97538del (TTN)	XP_024308866.1:p.Ser32513del
XM_024453099.1:c.79299_79301del (TTN)	XP_024308867.1:p.Ser26434del
XM_024453100.1:c.69153_69155del (TTN)	XP_024308868.1:p.Ser23052del