Canonical Allele Identifier: CA1310520637

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543314G= , CM000664.2:g.178543314G=	GRCh38
NC_000002.11:g.179408041G= , CM000664.1:g.179408041G=	GRCh37
NC_000002.10:g.179116287G=	NCBI36
NG_011618.3:g.292489C= , LRG_391:g.292489C=
NG_051363.1:g.25488G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88955C= (TTN)	ENSP00000343764.6:p.Thr29652=
ENST00000342175.11:c.70040C= (TTN)	ENSP00000340554.6:p.Thr23347=
ENST00000359218.10:c.69839C= (TTN)	ENSP00000352154.5:p.Thr23280=
ENST00000342175.10:c.70040C= (TTN)	ENSP00000340554.6:p.Thr23347=
ENST00000342992.10:c.88955C= (TTN)	ENSP00000343764.6:p.Thr29652=
ENST00000359218.9:c.69839C= (TTN)	ENSP00000352154.5:p.Thr23280=
ENST00000460472.6:c.69464C= (TTN)	ENSP00000434586.1:p.Thr23155=
ENST00000589042.5:c.96659C= (TTN) MANE Select	ENSP00000467141.1:p.Thr32220=
ENST00000591111.5:c.91736C= (TTN)	ENSP00000465570.1:p.Thr30579=
ENST00000615779.4:c.91736C= (TTN)	ENSP00000483597.1:p.Thr30579=
NM_001256850.1:c.91736C= (TTN)	NP_001243779.1:p.Thr30579=
NM_001267550.2:c.96659C= (TTN) MANE Select	NP_001254479.2:p.Thr32220=
NM_003319.4:c.69464C= (TTN)	NP_003310.4:p.Thr23155=
NM_133378.4:c.88955C= (TTN)	NP_596869.4:p.Thr29652=
NM_133432.3:c.69839C= (TTN)	NP_597676.3:p.Thr23280=
NM_133437.4:c.70040C= (TTN)	NP_597681.4:p.Thr23347=
NR_038271.1:n.446+19678G= (TTN-AS1)
NR_038272.1:n.2043+953G= (TTN-AS1)
XM_011511729.1:c.95756C= (TTN)	XP_011510031.1:p.Thr31919=
XM_011511730.1:c.69650C= (TTN)	XP_011510032.1:p.Thr23217=
XM_011511731.1:c.69509C= (TTN)	XP_011510033.1:p.Thr23170=
XM_017004819.1:c.95552C= (TTN)	XP_016860308.1:p.Thr31851=
XM_017004820.1:c.90950C= (TTN)	XP_016860309.1:p.Thr30317=
XM_017004821.1:c.90947C= (TTN)	XP_016860310.1:p.Thr30316=
XM_017004822.1:c.87989C= (TTN)	XP_016860311.1:p.Thr29330=
XM_017004823.1:c.69605C= (TTN)	XP_016860312.1:p.Thr23202=
XM_024453094.1:c.91100C= (TTN)	XP_024308862.1:p.Thr30367=
XM_024453095.1:c.91097C= (TTN)	XP_024308863.1:p.Thr30366=
XM_024453096.1:c.90530C= (TTN)	XP_024308864.1:p.Thr30177=
XM_024453097.1:c.87872C= (TTN)	XP_024308865.1:p.Thr29291=
XM_024453098.1:c.87791C= (TTN)	XP_024308866.1:p.Thr29264=
XM_024453099.1:c.69554C= (TTN)	XP_024308867.1:p.Thr23185=
XM_024453100.1:c.59408C= (TTN)	XP_024308868.1:p.Thr19803=