Canonical Allele Identifier: CA1310521107

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543836T= , CM000664.2:g.178543836T=	GRCh38
NC_000002.11:g.179408563T= , CM000664.1:g.179408563T=	GRCh37
NC_000002.10:g.179116809T=	NCBI36
NG_011618.3:g.291967A= , LRG_391:g.291967A=
NG_051363.1:g.26010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88604A= (TTN)	ENSP00000343764.6:p.Tyr29535=
ENST00000342175.11:c.69689A= (TTN)	ENSP00000340554.6:p.Tyr23230=
ENST00000359218.10:c.69488A= (TTN)	ENSP00000352154.5:p.Tyr23163=
ENST00000342175.10:c.69689A= (TTN)	ENSP00000340554.6:p.Tyr23230=
ENST00000342992.10:c.88604A= (TTN)	ENSP00000343764.6:p.Tyr29535=
ENST00000359218.9:c.69488A= (TTN)	ENSP00000352154.5:p.Tyr23163=
ENST00000460472.6:c.69113A= (TTN)	ENSP00000434586.1:p.Tyr23038=
ENST00000589042.5:c.96308A= (TTN) MANE Select	ENSP00000467141.1:p.Tyr32103=
ENST00000591111.5:c.91385A= (TTN)	ENSP00000465570.1:p.Tyr30462=
ENST00000615779.4:c.91385A= (TTN)	ENSP00000483597.1:p.Tyr30462=
NM_001256850.1:c.91385A= (TTN)	NP_001243779.1:p.Tyr30462=
NM_001267550.2:c.96308A= (TTN) MANE Select	NP_001254479.2:p.Tyr32103=
NM_003319.4:c.69113A= (TTN)	NP_003310.4:p.Tyr23038=
NM_133378.4:c.88604A= (TTN)	NP_596869.4:p.Tyr29535=
NM_133432.3:c.69488A= (TTN)	NP_597676.3:p.Tyr23163=
NM_133437.4:c.69689A= (TTN)	NP_597681.4:p.Tyr23230=
NR_038271.1:n.446+20200T= (TTN-AS1)
NR_038272.1:n.2043+1475T= (TTN-AS1)
XM_011511729.1:c.95405A= (TTN)	XP_011510031.1:p.Tyr31802=
XM_011511730.1:c.69299A= (TTN)	XP_011510032.1:p.Tyr23100=
XM_011511731.1:c.69158A= (TTN)	XP_011510033.1:p.Tyr23053=
XM_017004819.1:c.95201A= (TTN)	XP_016860308.1:p.Tyr31734=
XM_017004820.1:c.90599A= (TTN)	XP_016860309.1:p.Tyr30200=
XM_017004821.1:c.90596A= (TTN)	XP_016860310.1:p.Tyr30199=
XM_017004822.1:c.87638A= (TTN)	XP_016860311.1:p.Tyr29213=
XM_017004823.1:c.69254A= (TTN)	XP_016860312.1:p.Tyr23085=
XM_024453094.1:c.90749A= (TTN)	XP_024308862.1:p.Tyr30250=
XM_024453095.1:c.90746A= (TTN)	XP_024308863.1:p.Tyr30249=
XM_024453096.1:c.90179A= (TTN)	XP_024308864.1:p.Tyr30060=
XM_024453097.1:c.87521A= (TTN)	XP_024308865.1:p.Tyr29174=
XM_024453098.1:c.87440A= (TTN)	XP_024308866.1:p.Tyr29147=
XM_024453099.1:c.69203A= (TTN)	XP_024308867.1:p.Tyr23068=
XM_024453100.1:c.59057A= (TTN)	XP_024308868.1:p.Tyr19686=