Canonical Allele Identifier: CA1310551180

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618789C= , CM000664.2:g.178618789C=	GRCh38
NC_000002.11:g.179483516C= , CM000664.1:g.179483516C=	GRCh37
NC_000002.10:g.179191761C=	NCBI36
NG_011618.3:g.217014G= , LRG_391:g.217014G=
NG_051363.1:g.100963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39057G= (TTN)	ENSP00000343764.6:p.Met13019=
ENST00000342175.11:c.20142G= (TTN)	ENSP00000340554.6:p.Met6714=
ENST00000359218.10:c.19941G= (TTN)	ENSP00000352154.5:p.Met6647=
ENST00000342175.10:c.20142G= (TTN)	ENSP00000340554.6:p.Met6714=
ENST00000342992.10:c.39057G= (TTN)	ENSP00000343764.6:p.Met13019=
ENST00000359218.9:c.19941G= (TTN)	ENSP00000352154.5:p.Met6647=
ENST00000460472.6:c.19566G= (TTN)	ENSP00000434586.1:p.Met6522=
ENST00000589042.5:c.46761G= (TTN) MANE Select	ENSP00000467141.1:p.Met15587=
ENST00000591111.5:c.41838G= (TTN)	ENSP00000465570.1:p.Met13946=
ENST00000615779.4:c.41838G= (TTN)	ENSP00000483597.1:p.Met13946=
NM_001256850.1:c.41838G= (TTN)	NP_001243779.1:p.Met13946=
NM_001267550.2:c.46761G= (TTN) MANE Select	NP_001254479.2:p.Met15587=
NM_003319.4:c.19566G= (TTN)	NP_003310.4:p.Met6522=
NM_133378.4:c.39057G= (TTN)	NP_596869.4:p.Met13019=
NM_133432.3:c.19941G= (TTN)	NP_597676.3:p.Met6647=
NM_133437.4:c.20142G= (TTN)	NP_597681.4:p.Met6714=
NR_038271.1:n.1605-964C= (TTN-AS1)
XM_011511729.1:c.45858G= (TTN)	XP_011510031.1:p.Met15286=
XM_011511730.1:c.19752G= (TTN)	XP_011510032.1:p.Met6584=
XM_011511731.1:c.19611G= (TTN)	XP_011510033.1:p.Met6537=
XM_017004819.1:c.45654G= (TTN)	XP_016860308.1:p.Met15218=
XM_017004820.1:c.41052G= (TTN)	XP_016860309.1:p.Met13684=
XM_017004821.1:c.41049G= (TTN)	XP_016860310.1:p.Met13683=
XM_017004822.1:c.38091G= (TTN)	XP_016860311.1:p.Met12697=
XM_017004823.1:c.19707G= (TTN)	XP_016860312.1:p.Met6569=
XM_024453094.1:c.41202G= (TTN)	XP_024308862.1:p.Met13734=
XM_024453095.1:c.41199G= (TTN)	XP_024308863.1:p.Met13733=
XM_024453096.1:c.40632G= (TTN)	XP_024308864.1:p.Met13544=
XM_024453097.1:c.37974G= (TTN)	XP_024308865.1:p.Met12658=
XM_024453098.1:c.37893G= (TTN)	XP_024308866.1:p.Met12631=
XM_024453099.1:c.19656G= (TTN)	XP_024308867.1:p.Met6552=
XM_024453100.1:c.9510G= (TTN)	XP_024308868.1:p.Met3170=