Canonical Allele Identifier: CA1310534300

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577995G= , CM000664.2:g.178577995G=	GRCh38
NC_000002.11:g.179442722G= , CM000664.1:g.179442722G=	GRCh37
NC_000002.10:g.179150968G=	NCBI36
NG_011618.3:g.257808C= , LRG_391:g.257808C=
NG_051363.1:g.60169G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.60816C= (TTN)	ENSP00000343764.6:p.Asp20272=
ENST00000342175.11:c.41901C= (TTN)	ENSP00000340554.6:p.Asp13967=
ENST00000359218.10:c.41700C= (TTN)	ENSP00000352154.5:p.Asp13900=
ENST00000342175.10:c.41901C= (TTN)	ENSP00000340554.6:p.Asp13967=
ENST00000342992.10:c.60816C= (TTN)	ENSP00000343764.6:p.Asp20272=
ENST00000359218.9:c.41700C= (TTN)	ENSP00000352154.5:p.Asp13900=
ENST00000460472.6:c.41325C= (TTN)	ENSP00000434586.1:p.Asp13775=
ENST00000589042.5:c.68520C= (TTN) MANE Select	ENSP00000467141.1:p.Asp22840=
ENST00000591111.5:c.63597C= (TTN)	ENSP00000465570.1:p.Asp21199=
ENST00000615779.4:c.63597C= (TTN)	ENSP00000483597.1:p.Asp21199=
NM_001256850.1:c.63597C= (TTN)	NP_001243779.1:p.Asp21199=
NM_001267550.2:c.68520C= (TTN) MANE Select	NP_001254479.2:p.Asp22840=
NM_003319.4:c.41325C= (TTN)	NP_003310.4:p.Asp13775=
NM_133378.4:c.60816C= (TTN)	NP_596869.4:p.Asp20272=
NM_133432.3:c.41700C= (TTN)	NP_597676.3:p.Asp13900=
NM_133437.4:c.41901C= (TTN)	NP_597681.4:p.Asp13967=
NR_038271.1:n.596+6546G= (TTN-AS1)
NR_038272.1:n.2044-4577G= (TTN-AS1)
XM_011511729.1:c.67617C= (TTN)	XP_011510031.1:p.Asp22539=
XM_011511730.1:c.41511C= (TTN)	XP_011510032.1:p.Asp13837=
XM_011511731.1:c.41370C= (TTN)	XP_011510033.1:p.Asp13790=
XM_017004819.1:c.67413C= (TTN)	XP_016860308.1:p.Asp22471=
XM_017004820.1:c.62811C= (TTN)	XP_016860309.1:p.Asp20937=
XM_017004821.1:c.62808C= (TTN)	XP_016860310.1:p.Asp20936=
XM_017004822.1:c.59850C= (TTN)	XP_016860311.1:p.Asp19950=
XM_017004823.1:c.41466C= (TTN)	XP_016860312.1:p.Asp13822=
XM_024453094.1:c.62961C= (TTN)	XP_024308862.1:p.Asp20987=
XM_024453095.1:c.62958C= (TTN)	XP_024308863.1:p.Asp20986=
XM_024453096.1:c.62391C= (TTN)	XP_024308864.1:p.Asp20797=
XM_024453097.1:c.59733C= (TTN)	XP_024308865.1:p.Asp19911=
XM_024453098.1:c.59652C= (TTN)	XP_024308866.1:p.Asp19884=
XM_024453099.1:c.41415C= (TTN)	XP_024308867.1:p.Asp13805=
XM_024453100.1:c.31269C= (TTN)	XP_024308868.1:p.Asp10423=