Canonical Allele Identifier: CA349480237

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547773T>A , CM000664.2:g.178547773T>A	GRCh38
NC_000002.11:g.179412500T>A , CM000664.1:g.179412500T>A	GRCh37
NC_000002.10:g.179120746T>A	NCBI36
NG_011618.3:g.288030A>T , LRG_391:g.288030A>T
NG_051363.1:g.29947T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.93853A>T (TTN) MANE Select	NP_001254479.2:p.Arg31285Ter
ENST00000589042.5:c.93853A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg31285Ter
NM_001256850.1:c.88930A>T (TTN)	NP_001243779.1:p.Arg29644Ter
NM_003319.4:c.66658A>T (TTN)	NP_003310.4:p.Arg22220Ter
NM_133378.4:c.86149A>T (TTN)	NP_596869.4:p.Arg28717Ter
NM_133432.3:c.67033A>T (TTN)	NP_597676.3:p.Arg22345Ter
NM_133437.4:c.67234A>T (TTN)	NP_597681.4:p.Arg22412Ter
NR_038271.1:n.447-23527T>A (TTN-AS1)
NR_038272.1:n.2043+5412T>A (TTN-AS1)
ENST00000342175.10:c.67234A>T (TTN)	ENSP00000340554.6:p.Arg22412Ter
ENST00000342175.11:c.67234A>T (TTN)	ENSP00000340554.6:p.Arg22412Ter
ENST00000342992.10:c.86149A>T (TTN)	ENSP00000343764.6:p.Arg28717Ter
ENST00000342992.11:c.86149A>T (TTN)	ENSP00000343764.6:p.Arg28717Ter
ENST00000359218.10:c.67033A>T (TTN)	ENSP00000352154.5:p.Arg22345Ter
ENST00000359218.9:c.67033A>T (TTN)	ENSP00000352154.5:p.Arg22345Ter
ENST00000460472.6:c.66658A>T (TTN)	ENSP00000434586.1:p.Arg22220Ter
ENST00000591111.5:c.88930A>T (TTN)	ENSP00000465570.1:p.Arg29644Ter
ENST00000615779.4:c.88930A>T (TTN)	ENSP00000483597.1:p.Arg29644Ter
XM_011511729.1:c.92950A>T (TTN)	XP_011510031.1:p.Arg30984Ter
XM_011511730.1:c.66844A>T (TTN)	XP_011510032.1:p.Arg22282Ter
XM_011511731.1:c.66703A>T (TTN)	XP_011510033.1:p.Arg22235Ter
XM_017004819.1:c.92746A>T (TTN)	XP_016860308.1:p.Arg30916Ter
XM_017004820.1:c.88144A>T (TTN)	XP_016860309.1:p.Arg29382Ter
XM_017004821.1:c.88141A>T (TTN)	XP_016860310.1:p.Arg29381Ter
XM_017004822.1:c.85183A>T (TTN)	XP_016860311.1:p.Arg28395Ter
XM_017004823.1:c.66799A>T (TTN)	XP_016860312.1:p.Arg22267Ter
XM_024453094.1:c.88294A>T (TTN)	XP_024308862.1:p.Arg29432Ter
XM_024453095.1:c.88291A>T (TTN)	XP_024308863.1:p.Arg29431Ter
XM_024453096.1:c.87724A>T (TTN)	XP_024308864.1:p.Arg29242Ter
XM_024453097.1:c.85066A>T (TTN)	XP_024308865.1:p.Arg28356Ter
XM_024453098.1:c.84985A>T (TTN)	XP_024308866.1:p.Arg28329Ter
XM_024453099.1:c.66748A>T (TTN)	XP_024308867.1:p.Arg22250Ter
XM_024453100.1:c.56602A>T (TTN)	XP_024308868.1:p.Arg18868Ter