Canonical Allele Identifier: CA349427930

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179402362T>C (hg19) ; chr2:g.178537635T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537635T>C , CM000664.2:g.178537635T>C	GRCh38
NC_000002.11:g.179402362T>C , CM000664.1:g.179402362T>C	GRCh37
NC_000002.10:g.179110608T>C	NCBI36
NG_011618.3:g.298168A>G , LRG_391:g.298168A>G
NG_051363.1:g.19809T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.91868A>G (TTN)	ENSP00000343764.6:p.Gln30623Arg
ENST00000342175.11:c.72953A>G (TTN)	ENSP00000340554.6:p.Gln24318Arg
ENST00000359218.10:c.72752A>G (TTN)	ENSP00000352154.5:p.Gln24251Arg
ENST00000342175.10:c.72953A>G (TTN)	ENSP00000340554.6:p.Gln24318Arg
ENST00000342992.10:c.91868A>G (TTN)	ENSP00000343764.6:p.Gln30623Arg
ENST00000359218.9:c.72752A>G (TTN)	ENSP00000352154.5:p.Gln24251Arg
ENST00000460472.6:c.72377A>G (TTN)	ENSP00000434586.1:p.Gln24126Arg
ENST00000589042.5:c.99572A>G (TTN) MANE Select	ENSP00000467141.1:p.Gln33191Arg
ENST00000591111.5:c.94649A>G (TTN)	ENSP00000465570.1:p.Gln31550Arg
ENST00000615779.4:c.94649A>G (TTN)	ENSP00000483597.1:p.Gln31550Arg
NM_001256850.1:c.94649A>G (TTN)	NP_001243779.1:p.Gln31550Arg
NM_001267550.2:c.99572A>G (TTN) MANE Select	NP_001254479.2:p.Gln33191Arg
NM_003319.4:c.72377A>G (TTN)	NP_003310.4:p.Gln24126Arg
NM_133378.4:c.91868A>G (TTN)	NP_596869.4:p.Gln30623Arg
NM_133432.3:c.72752A>G (TTN)	NP_597676.3:p.Gln24251Arg
NM_133437.4:c.72953A>G (TTN)	NP_597681.4:p.Gln24318Arg
NR_038271.1:n.446+13999T>C (TTN-AS1)
NR_038272.1:n.591T>C (TTN-AS1)
XM_011511729.1:c.98669A>G (TTN)	XP_011510031.1:p.Gln32890Arg
XM_011511730.1:c.72563A>G (TTN)	XP_011510032.1:p.Gln24188Arg
XM_011511731.1:c.72422A>G (TTN)	XP_011510033.1:p.Gln24141Arg
XM_017004819.1:c.98465A>G (TTN)	XP_016860308.1:p.Gln32822Arg
XM_017004820.1:c.93863A>G (TTN)	XP_016860309.1:p.Gln31288Arg
XM_017004821.1:c.93860A>G (TTN)	XP_016860310.1:p.Gln31287Arg
XM_017004822.1:c.90902A>G (TTN)	XP_016860311.1:p.Gln30301Arg
XM_017004823.1:c.72518A>G (TTN)	XP_016860312.1:p.Gln24173Arg
XM_024453094.1:c.94013A>G (TTN)	XP_024308862.1:p.Gln31338Arg
XM_024453095.1:c.94010A>G (TTN)	XP_024308863.1:p.Gln31337Arg
XM_024453096.1:c.93443A>G (TTN)	XP_024308864.1:p.Gln31148Arg
XM_024453097.1:c.90785A>G (TTN)	XP_024308865.1:p.Gln30262Arg
XM_024453098.1:c.90704A>G (TTN)	XP_024308866.1:p.Gln30235Arg
XM_024453099.1:c.72467A>G (TTN)	XP_024308867.1:p.Gln24156Arg
XM_024453100.1:c.62321A>G (TTN)	XP_024308868.1:p.Gln20774Arg