Canonical Allele Identifier: CA1310514737

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1688654818

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530551_178530553del , CM000664.2:g.178530551_178530553del	GRCh38
NC_000002.11:g.179395278_179395280del , CM000664.1:g.179395278_179395280del	GRCh37
NC_000002.10:g.179103524_179103526del	NCBI36
NG_011618.3:g.305252_305254del , LRG_391:g.305252_305254del
NG_051363.1:g.12725_12727del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98360_98362del (TTN)	ENSP00000343764.6:p.Gly32787del
ENST00000342175.11:c.79445_79447del (TTN)	ENSP00000340554.6:p.Gly26482del
ENST00000359218.10:c.79244_79246del (TTN)	ENSP00000352154.5:p.Gly26415del
ENST00000342175.10:c.79445_79447del (TTN)	ENSP00000340554.6:p.Gly26482del
ENST00000342992.10:c.98360_98362del (TTN)	ENSP00000343764.6:p.Gly32787del
ENST00000359218.9:c.79244_79246del (TTN)	ENSP00000352154.5:p.Gly26415del
ENST00000460472.6:c.78869_78871del (TTN)	ENSP00000434586.1:p.Gly26290del
ENST00000589042.5:c.106064_106066del (TTN) MANE Select	ENSP00000467141.1:p.Gly35355del
ENST00000591111.5:c.101141_101143del (TTN)	ENSP00000465570.1:p.Gly33714del
ENST00000615779.4:c.101141_101143del (TTN)	ENSP00000483597.1:p.Gly33714del
NM_001256850.1:c.101141_101143del (TTN)	NP_001243779.1:p.Gly33714del
NM_001267550.2:c.106064_106066del (TTN) MANE Select	NP_001254479.2:p.Gly35355del
NM_003319.4:c.78869_78871del (TTN)	NP_003310.4:p.Gly26290del
NM_133378.4:c.98360_98362del (TTN)	NP_596869.4:p.Gly32787del
NM_133432.3:c.79244_79246del (TTN)	NP_597676.3:p.Gly26415del
NM_133437.4:c.79445_79447del (TTN)	NP_597681.4:p.Gly26482del
NR_038271.1:n.446+6915_446+6917del (TTN-AS1)
NR_038272.1:n.220-5181_220-5179del (TTN-AS1)
XM_011511729.1:c.105161_105163del (TTN)	XP_011510031.1:p.Gly35054del
XM_011511730.1:c.79055_79057del (TTN)	XP_011510032.1:p.Gly26352del
XM_011511731.1:c.78914_78916del (TTN)	XP_011510033.1:p.Gly26305del
XM_017004819.1:c.104957_104959del (TTN)	XP_016860308.1:p.Gly34986del
XM_017004820.1:c.100355_100357del (TTN)	XP_016860309.1:p.Gly33452del
XM_017004821.1:c.100352_100354del (TTN)	XP_016860310.1:p.Gly33451del
XM_017004822.1:c.97394_97396del (TTN)	XP_016860311.1:p.Gly32465del
XM_017004823.1:c.79010_79012del (TTN)	XP_016860312.1:p.Gly26337del
XM_024453094.1:c.100505_100507del (TTN)	XP_024308862.1:p.Gly33502del
XM_024453095.1:c.100502_100504del (TTN)	XP_024308863.1:p.Gly33501del
XM_024453096.1:c.99935_99937del (TTN)	XP_024308864.1:p.Gly33312del
XM_024453097.1:c.97277_97279del (TTN)	XP_024308865.1:p.Gly32426del
XM_024453098.1:c.97196_97198del (TTN)	XP_024308866.1:p.Gly32399del
XM_024453099.1:c.78959_78961del (TTN)	XP_024308867.1:p.Gly26320del
XM_024453100.1:c.68813_68815del (TTN)	XP_024308868.1:p.Gly22938del