Canonical Allele Identifier: CA349436974

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179449606C>G (hg19) ; chr2:g.178584879C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584879C>G , CM000664.2:g.178584879C>G	GRCh38
NC_000002.11:g.179449606C>G , CM000664.1:g.179449606C>G	GRCh37
NC_000002.10:g.179157852C>G	NCBI36
NG_011618.3:g.250924G>C , LRG_391:g.250924G>C
NG_051363.1:g.67053C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.57058G>C (TTN)	ENSP00000343764.6:p.Gly19020Arg
ENST00000342175.11:c.38143G>C (TTN)	ENSP00000340554.6:p.Gly12715Arg
ENST00000359218.10:c.37942G>C (TTN)	ENSP00000352154.5:p.Gly12648Arg
ENST00000342175.10:c.38143G>C (TTN)	ENSP00000340554.6:p.Gly12715Arg
ENST00000342992.10:c.57058G>C (TTN)	ENSP00000343764.6:p.Gly19020Arg
ENST00000359218.9:c.37942G>C (TTN)	ENSP00000352154.5:p.Gly12648Arg
ENST00000460472.6:c.37567G>C (TTN)	ENSP00000434586.1:p.Gly12523Arg
ENST00000589042.5:c.64762G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly21588Arg
ENST00000591111.5:c.59839G>C (TTN)	ENSP00000465570.1:p.Gly19947Arg
ENST00000615779.4:c.59839G>C (TTN)	ENSP00000483597.1:p.Gly19947Arg
NM_001256850.1:c.59839G>C (TTN)	NP_001243779.1:p.Gly19947Arg
NM_001267550.2:c.64762G>C (TTN) MANE Select	NP_001254479.2:p.Gly21588Arg
NM_003319.4:c.37567G>C (TTN)	NP_003310.4:p.Gly12523Arg
NM_133378.4:c.57058G>C (TTN)	NP_596869.4:p.Gly19020Arg
NM_133432.3:c.37942G>C (TTN)	NP_597676.3:p.Gly12648Arg
NM_133437.4:c.38143G>C (TTN)	NP_597681.4:p.Gly12715Arg
NR_038271.1:n.597-12717C>G (TTN-AS1)
NR_038272.1:n.3074C>G (TTN-AS1)
XM_011511729.1:c.63859G>C (TTN)	XP_011510031.1:p.Gly21287Arg
XM_011511730.1:c.37753G>C (TTN)	XP_011510032.1:p.Gly12585Arg
XM_011511731.1:c.37612G>C (TTN)	XP_011510033.1:p.Gly12538Arg
XM_017004819.1:c.63655G>C (TTN)	XP_016860308.1:p.Gly21219Arg
XM_017004820.1:c.59053G>C (TTN)	XP_016860309.1:p.Gly19685Arg
XM_017004821.1:c.59050G>C (TTN)	XP_016860310.1:p.Gly19684Arg
XM_017004822.1:c.56092G>C (TTN)	XP_016860311.1:p.Gly18698Arg
XM_017004823.1:c.37708G>C (TTN)	XP_016860312.1:p.Gly12570Arg
XM_024453094.1:c.59203G>C (TTN)	XP_024308862.1:p.Gly19735Arg
XM_024453095.1:c.59200G>C (TTN)	XP_024308863.1:p.Gly19734Arg
XM_024453096.1:c.58633G>C (TTN)	XP_024308864.1:p.Gly19545Arg
XM_024453097.1:c.55975G>C (TTN)	XP_024308865.1:p.Gly18659Arg
XM_024453098.1:c.55894G>C (TTN)	XP_024308866.1:p.Gly18632Arg
XM_024453099.1:c.37657G>C (TTN)	XP_024308867.1:p.Gly12553Arg
XM_024453100.1:c.27511G>C (TTN)	XP_024308868.1:p.Gly9171Arg