Canonical Allele Identifier: CA349443013

Gene: TTN TTN-AS1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586712T>A , CM000664.2:g.178586712T>A	GRCh38
NC_000002.11:g.179451439T>A , CM000664.1:g.179451439T>A	GRCh37
NC_000002.10:g.179159685T>A	NCBI36
NG_011618.3:g.249091A>T , LRG_391:g.249091A>T
NG_051363.1:g.68886T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.56485A>T (TTN)	ENSP00000343764.6:p.Lys18829Ter
ENST00000342175.11:c.37570A>T (TTN)	ENSP00000340554.6:p.Lys12524Ter
ENST00000359218.10:c.37369A>T (TTN)	ENSP00000352154.5:p.Lys12457Ter
ENST00000342175.10:c.37570A>T (TTN)	ENSP00000340554.6:p.Lys12524Ter
ENST00000342992.10:c.56485A>T (TTN)	ENSP00000343764.6:p.Lys18829Ter
ENST00000359218.9:c.37369A>T (TTN)	ENSP00000352154.5:p.Lys12457Ter
ENST00000460472.6:c.36994A>T (TTN)	ENSP00000434586.1:p.Lys12332Ter
ENST00000589042.5:c.64189A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys21397Ter
ENST00000591111.5:c.59266A>T (TTN)	ENSP00000465570.1:p.Lys19756Ter
ENST00000615779.4:c.59266A>T (TTN)	ENSP00000483597.1:p.Lys19756Ter
NM_001256850.1:c.59266A>T (TTN)	NP_001243779.1:p.Lys19756Ter
NM_001267550.2:c.64189A>T (TTN) MANE Select	NP_001254479.2:p.Lys21397Ter
NM_003319.4:c.36994A>T (TTN)	NP_003310.4:p.Lys12332Ter
NM_133378.4:c.56485A>T (TTN)	NP_596869.4:p.Lys18829Ter
NM_133432.3:c.37369A>T (TTN)	NP_597676.3:p.Lys12457Ter
NM_133437.4:c.37570A>T (TTN)	NP_597681.4:p.Lys12524Ter
NR_038271.1:n.597-10884T>A (TTN-AS1)
NR_038272.1:n.3188+1719T>A (TTN-AS1)
XM_011511729.1:c.63286A>T (TTN)	XP_011510031.1:p.Lys21096Ter
XM_011511730.1:c.37180A>T (TTN)	XP_011510032.1:p.Lys12394Ter
XM_011511731.1:c.37039A>T (TTN)	XP_011510033.1:p.Lys12347Ter
XM_017004819.1:c.63082A>T (TTN)	XP_016860308.1:p.Lys21028Ter
XM_017004820.1:c.58480A>T (TTN)	XP_016860309.1:p.Lys19494Ter
XM_017004821.1:c.58477A>T (TTN)	XP_016860310.1:p.Lys19493Ter
XM_017004822.1:c.55519A>T (TTN)	XP_016860311.1:p.Lys18507Ter
XM_017004823.1:c.37135A>T (TTN)	XP_016860312.1:p.Lys12379Ter
XM_024453094.1:c.58630A>T (TTN)	XP_024308862.1:p.Lys19544Ter
XM_024453095.1:c.58627A>T (TTN)	XP_024308863.1:p.Lys19543Ter
XM_024453096.1:c.58060A>T (TTN)	XP_024308864.1:p.Lys19354Ter
XM_024453097.1:c.55402A>T (TTN)	XP_024308865.1:p.Lys18468Ter
XM_024453098.1:c.55321A>T (TTN)	XP_024308866.1:p.Lys18441Ter
XM_024453099.1:c.37084A>T (TTN)	XP_024308867.1:p.Lys12362Ter
XM_024453100.1:c.26938A>T (TTN)	XP_024308868.1:p.Lys8980Ter