Canonical Allele Identifier: CA1310521122

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551633C= , CM000664.2:g.178551633C=	GRCh38
NC_000002.11:g.179416360C= , CM000664.1:g.179416360C=	GRCh37
NC_000002.10:g.179124606C=	NCBI36
NG_011618.3:g.284170G= , LRG_391:g.284170G=
NG_051363.1:g.33807C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.83563G= (TTN)	ENSP00000343764.6:p.Val27855=
ENST00000342175.11:c.64648G= (TTN)	ENSP00000340554.6:p.Val21550=
ENST00000359218.10:c.64447G= (TTN)	ENSP00000352154.5:p.Val21483=
ENST00000342175.10:c.64648G= (TTN)	ENSP00000340554.6:p.Val21550=
ENST00000342992.10:c.83563G= (TTN)	ENSP00000343764.6:p.Val27855=
ENST00000359218.9:c.64447G= (TTN)	ENSP00000352154.5:p.Val21483=
ENST00000460472.6:c.64072G= (TTN)	ENSP00000434586.1:p.Val21358=
ENST00000589042.5:c.91267G= (TTN) MANE Select	ENSP00000467141.1:p.Val30423=
ENST00000591111.5:c.86344G= (TTN)	ENSP00000465570.1:p.Val28782=
ENST00000615779.4:c.86344G= (TTN)	ENSP00000483597.1:p.Val28782=
NM_001256850.1:c.86344G= (TTN)	NP_001243779.1:p.Val28782=
NM_001267550.2:c.91267G= (TTN) MANE Select	NP_001254479.2:p.Val30423=
NM_003319.4:c.64072G= (TTN)	NP_003310.4:p.Val21358=
NM_133378.4:c.83563G= (TTN)	NP_596869.4:p.Val27855=
NM_133432.3:c.64447G= (TTN)	NP_597676.3:p.Val21483=
NM_133437.4:c.64648G= (TTN)	NP_597681.4:p.Val21550=
NR_038271.1:n.447-19667C= (TTN-AS1)
NR_038272.1:n.2043+9272C= (TTN-AS1)
XM_011511729.1:c.90364G= (TTN)	XP_011510031.1:p.Val30122=
XM_011511730.1:c.64258G= (TTN)	XP_011510032.1:p.Val21420=
XM_011511731.1:c.64117G= (TTN)	XP_011510033.1:p.Val21373=
XM_017004819.1:c.90160G= (TTN)	XP_016860308.1:p.Val30054=
XM_017004820.1:c.85558G= (TTN)	XP_016860309.1:p.Val28520=
XM_017004821.1:c.85555G= (TTN)	XP_016860310.1:p.Val28519=
XM_017004822.1:c.82597G= (TTN)	XP_016860311.1:p.Val27533=
XM_017004823.1:c.64213G= (TTN)	XP_016860312.1:p.Val21405=
XM_024453094.1:c.85708G= (TTN)	XP_024308862.1:p.Val28570=
XM_024453095.1:c.85705G= (TTN)	XP_024308863.1:p.Val28569=
XM_024453096.1:c.85138G= (TTN)	XP_024308864.1:p.Val28380=
XM_024453097.1:c.82480G= (TTN)	XP_024308865.1:p.Val27494=
XM_024453098.1:c.82399G= (TTN)	XP_024308866.1:p.Val27467=
XM_024453099.1:c.64162G= (TTN)	XP_024308867.1:p.Val21388=
XM_024453100.1:c.54016G= (TTN)	XP_024308868.1:p.Val18006=