Canonical Allele Identifier: CA349456554

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544357G>A , CM000664.2:g.178544357G>A	GRCh38
NC_000002.11:g.179409084G>A , CM000664.1:g.179409084G>A	GRCh37
NC_000002.10:g.179117330G>A	NCBI36
NG_011618.3:g.291446C>T , LRG_391:g.291446C>T
NG_051363.1:g.26531G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.95872C>T (TTN) MANE Select	NP_001254479.2:p.Arg31958Ter
ENST00000589042.5:c.95872C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg31958Ter
NM_001256850.1:c.90949C>T (TTN)	NP_001243779.1:p.Arg30317Ter
NM_003319.4:c.68677C>T (TTN)	NP_003310.4:p.Arg22893Ter
NM_133378.4:c.88168C>T (TTN)	NP_596869.4:p.Arg29390Ter
NM_133432.3:c.69052C>T (TTN)	NP_597676.3:p.Arg23018Ter
NM_133437.4:c.69253C>T (TTN)	NP_597681.4:p.Arg23085Ter
NR_038271.1:n.446+20721G>A (TTN-AS1)
NR_038272.1:n.2043+1996G>A (TTN-AS1)
ENST00000342175.10:c.69253C>T (TTN)	ENSP00000340554.6:p.Arg23085Ter
ENST00000342175.11:c.69253C>T (TTN)	ENSP00000340554.6:p.Arg23085Ter
ENST00000342992.10:c.88168C>T (TTN)	ENSP00000343764.6:p.Arg29390Ter
ENST00000342992.11:c.88168C>T (TTN)	ENSP00000343764.6:p.Arg29390Ter
ENST00000359218.10:c.69052C>T (TTN)	ENSP00000352154.5:p.Arg23018Ter
ENST00000359218.9:c.69052C>T (TTN)	ENSP00000352154.5:p.Arg23018Ter
ENST00000460472.6:c.68677C>T (TTN)	ENSP00000434586.1:p.Arg22893Ter
ENST00000591111.5:c.90949C>T (TTN)	ENSP00000465570.1:p.Arg30317Ter
ENST00000615779.4:c.90949C>T (TTN)	ENSP00000483597.1:p.Arg30317Ter
XM_011511729.1:c.94969C>T (TTN)	XP_011510031.1:p.Arg31657Ter
XM_011511730.1:c.68863C>T (TTN)	XP_011510032.1:p.Arg22955Ter
XM_011511731.1:c.68722C>T (TTN)	XP_011510033.1:p.Arg22908Ter
XM_017004819.1:c.94765C>T (TTN)	XP_016860308.1:p.Arg31589Ter
XM_017004820.1:c.90163C>T (TTN)	XP_016860309.1:p.Arg30055Ter
XM_017004821.1:c.90160C>T (TTN)	XP_016860310.1:p.Arg30054Ter
XM_017004822.1:c.87202C>T (TTN)	XP_016860311.1:p.Arg29068Ter
XM_017004823.1:c.68818C>T (TTN)	XP_016860312.1:p.Arg22940Ter
XM_024453094.1:c.90313C>T (TTN)	XP_024308862.1:p.Arg30105Ter
XM_024453095.1:c.90310C>T (TTN)	XP_024308863.1:p.Arg30104Ter
XM_024453096.1:c.89743C>T (TTN)	XP_024308864.1:p.Arg29915Ter
XM_024453097.1:c.87085C>T (TTN)	XP_024308865.1:p.Arg29029Ter
XM_024453098.1:c.87004C>T (TTN)	XP_024308866.1:p.Arg29002Ter
XM_024453099.1:c.68767C>T (TTN)	XP_024308867.1:p.Arg22923Ter
XM_024453100.1:c.58621C>T (TTN)	XP_024308868.1:p.Arg19541Ter