Canonical Allele Identifier: CA349512586

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1575521744
• MyVariant Identifiers: chr2:g.179417385C>T (hg19) ; chr2:g.178552658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552658C>T , CM000664.2:g.178552658C>T	GRCh38
NC_000002.11:g.179417385C>T , CM000664.1:g.179417385C>T	GRCh37
NC_000002.10:g.179125631C>T	NCBI36
NG_011618.3:g.283145G>A , LRG_391:g.283145G>A
NG_051363.1:g.34832C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82538G>A (TTN)	ENSP00000343764.6:p.Gly27513Asp
ENST00000342175.11:c.63623G>A (TTN)	ENSP00000340554.6:p.Gly21208Asp
ENST00000359218.10:c.63422G>A (TTN)	ENSP00000352154.5:p.Gly21141Asp
ENST00000342175.10:c.63623G>A (TTN)	ENSP00000340554.6:p.Gly21208Asp
ENST00000342992.10:c.82538G>A (TTN)	ENSP00000343764.6:p.Gly27513Asp
ENST00000359218.9:c.63422G>A (TTN)	ENSP00000352154.5:p.Gly21141Asp
ENST00000460472.6:c.63047G>A (TTN)	ENSP00000434586.1:p.Gly21016Asp
ENST00000589042.5:c.90242G>A (TTN) MANE Select	ENSP00000467141.1:p.Gly30081Asp
ENST00000591111.5:c.85319G>A (TTN)	ENSP00000465570.1:p.Gly28440Asp
ENST00000615779.4:c.85319G>A (TTN)	ENSP00000483597.1:p.Gly28440Asp
NM_001256850.1:c.85319G>A (TTN)	NP_001243779.1:p.Gly28440Asp
NM_001267550.2:c.90242G>A (TTN) MANE Select	NP_001254479.2:p.Gly30081Asp
NM_003319.4:c.63047G>A (TTN)	NP_003310.4:p.Gly21016Asp
NM_133378.4:c.82538G>A (TTN)	NP_596869.4:p.Gly27513Asp
NM_133432.3:c.63422G>A (TTN)	NP_597676.3:p.Gly21141Asp
NM_133437.4:c.63623G>A (TTN)	NP_597681.4:p.Gly21208Asp
NR_038271.1:n.447-18642C>T (TTN-AS1)
NR_038272.1:n.2043+10297C>T (TTN-AS1)
XM_011511729.1:c.89339G>A (TTN)	XP_011510031.1:p.Gly29780Asp
XM_011511730.1:c.63233G>A (TTN)	XP_011510032.1:p.Gly21078Asp
XM_011511731.1:c.63092G>A (TTN)	XP_011510033.1:p.Gly21031Asp
XM_017004819.1:c.89135G>A (TTN)	XP_016860308.1:p.Gly29712Asp
XM_017004820.1:c.84533G>A (TTN)	XP_016860309.1:p.Gly28178Asp
XM_017004821.1:c.84530G>A (TTN)	XP_016860310.1:p.Gly28177Asp
XM_017004822.1:c.81572G>A (TTN)	XP_016860311.1:p.Gly27191Asp
XM_017004823.1:c.63188G>A (TTN)	XP_016860312.1:p.Gly21063Asp
XM_024453094.1:c.84683G>A (TTN)	XP_024308862.1:p.Gly28228Asp
XM_024453095.1:c.84680G>A (TTN)	XP_024308863.1:p.Gly28227Asp
XM_024453096.1:c.84113G>A (TTN)	XP_024308864.1:p.Gly28038Asp
XM_024453097.1:c.81455G>A (TTN)	XP_024308865.1:p.Gly27152Asp
XM_024453098.1:c.81374G>A (TTN)	XP_024308866.1:p.Gly27125Asp
XM_024453099.1:c.63137G>A (TTN)	XP_024308867.1:p.Gly21046Asp
XM_024453100.1:c.52991G>A (TTN)	XP_024308868.1:p.Gly17664Asp