Canonical Allele Identifier: CA1310522704

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546050C= , CM000664.2:g.178546050C=	GRCh38
NC_000002.11:g.179410777C= , CM000664.1:g.179410777C=	GRCh37
NC_000002.10:g.179119023C=	NCBI36
NG_011618.3:g.289753G= , LRG_391:g.289753G=
NG_051363.1:g.28224C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.95186G= (TTN) MANE Select	NP_001254479.2:p.Trp31729=
ENST00000589042.5:c.95186G= (TTN) MANE Select	ENSP00000467141.1:p.Trp31729=
NM_001256850.1:c.90263G= (TTN)	NP_001243779.1:p.Trp30088=
NM_003319.4:c.67991G= (TTN)	NP_003310.4:p.Trp22664=
NM_133378.4:c.87482G= (TTN)	NP_596869.4:p.Trp29161=
NM_133432.3:c.68366G= (TTN)	NP_597676.3:p.Trp22789=
NM_133437.4:c.68567G= (TTN)	NP_597681.4:p.Trp22856=
NR_038271.1:n.446+22414C= (TTN-AS1)
NR_038272.1:n.2043+3689C= (TTN-AS1)
ENST00000342175.10:c.68567G= (TTN)	ENSP00000340554.6:p.Trp22856=
ENST00000342175.11:c.68567G= (TTN)	ENSP00000340554.6:p.Trp22856=
ENST00000342992.10:c.87482G= (TTN)	ENSP00000343764.6:p.Trp29161=
ENST00000342992.11:c.87482G= (TTN)	ENSP00000343764.6:p.Trp29161=
ENST00000359218.10:c.68366G= (TTN)	ENSP00000352154.5:p.Trp22789=
ENST00000359218.9:c.68366G= (TTN)	ENSP00000352154.5:p.Trp22789=
ENST00000460472.6:c.67991G= (TTN)	ENSP00000434586.1:p.Trp22664=
ENST00000591111.5:c.90263G= (TTN)	ENSP00000465570.1:p.Trp30088=
ENST00000615779.4:c.90263G= (TTN)	ENSP00000483597.1:p.Trp30088=
XM_011511729.1:c.94283G= (TTN)	XP_011510031.1:p.Trp31428=
XM_011511730.1:c.68177G= (TTN)	XP_011510032.1:p.Trp22726=
XM_011511731.1:c.68036G= (TTN)	XP_011510033.1:p.Trp22679=
XM_017004819.1:c.94079G= (TTN)	XP_016860308.1:p.Trp31360=
XM_017004820.1:c.89477G= (TTN)	XP_016860309.1:p.Trp29826=
XM_017004821.1:c.89474G= (TTN)	XP_016860310.1:p.Trp29825=
XM_017004822.1:c.86516G= (TTN)	XP_016860311.1:p.Trp28839=
XM_017004823.1:c.68132G= (TTN)	XP_016860312.1:p.Trp22711=
XM_024453094.1:c.89627G= (TTN)	XP_024308862.1:p.Trp29876=
XM_024453095.1:c.89624G= (TTN)	XP_024308863.1:p.Trp29875=
XM_024453096.1:c.89057G= (TTN)	XP_024308864.1:p.Trp29686=
XM_024453097.1:c.86399G= (TTN)	XP_024308865.1:p.Trp28800=
XM_024453098.1:c.86318G= (TTN)	XP_024308866.1:p.Trp28773=
XM_024453099.1:c.68081G= (TTN)	XP_024308867.1:p.Trp22694=
XM_024453100.1:c.57935G= (TTN)	XP_024308868.1:p.Trp19312=