Canonical Allele Identifier: CA349432636

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179447736C>G (hg19) ; chr2:g.178583009C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178583009C>G , CM000664.2:g.178583009C>G	GRCh38
NC_000002.11:g.179447736C>G , CM000664.1:g.179447736C>G	GRCh37
NC_000002.10:g.179155982C>G	NCBI36
NG_011618.3:g.252794G>C , LRG_391:g.252794G>C
NG_051363.1:g.65183C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.58090G>C (TTN)	ENSP00000343764.6:p.Gly19364Arg
ENST00000342175.11:c.39175G>C (TTN)	ENSP00000340554.6:p.Gly13059Arg
ENST00000359218.10:c.38974G>C (TTN)	ENSP00000352154.5:p.Gly12992Arg
ENST00000342175.10:c.39175G>C (TTN)	ENSP00000340554.6:p.Gly13059Arg
ENST00000342992.10:c.58090G>C (TTN)	ENSP00000343764.6:p.Gly19364Arg
ENST00000359218.9:c.38974G>C (TTN)	ENSP00000352154.5:p.Gly12992Arg
ENST00000460472.6:c.38599G>C (TTN)	ENSP00000434586.1:p.Gly12867Arg
ENST00000589042.5:c.65794G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly21932Arg
ENST00000591111.5:c.60871G>C (TTN)	ENSP00000465570.1:p.Gly20291Arg
ENST00000615779.4:c.60871G>C (TTN)	ENSP00000483597.1:p.Gly20291Arg
NM_001256850.1:c.60871G>C (TTN)	NP_001243779.1:p.Gly20291Arg
NM_001267550.2:c.65794G>C (TTN) MANE Select	NP_001254479.2:p.Gly21932Arg
NM_003319.4:c.38599G>C (TTN)	NP_003310.4:p.Gly12867Arg
NM_133378.4:c.58090G>C (TTN)	NP_596869.4:p.Gly19364Arg
NM_133432.3:c.38974G>C (TTN)	NP_597676.3:p.Gly12992Arg
NM_133437.4:c.39175G>C (TTN)	NP_597681.4:p.Gly13059Arg
NR_038271.1:n.596+11560C>G (TTN-AS1)
NR_038272.1:n.2197C>G (TTN-AS1)
XM_011511729.1:c.64891G>C (TTN)	XP_011510031.1:p.Gly21631Arg
XM_011511730.1:c.38785G>C (TTN)	XP_011510032.1:p.Gly12929Arg
XM_011511731.1:c.38644G>C (TTN)	XP_011510033.1:p.Gly12882Arg
XM_017004819.1:c.64687G>C (TTN)	XP_016860308.1:p.Gly21563Arg
XM_017004820.1:c.60085G>C (TTN)	XP_016860309.1:p.Gly20029Arg
XM_017004821.1:c.60082G>C (TTN)	XP_016860310.1:p.Gly20028Arg
XM_017004822.1:c.57124G>C (TTN)	XP_016860311.1:p.Gly19042Arg
XM_017004823.1:c.38740G>C (TTN)	XP_016860312.1:p.Gly12914Arg
XM_024453094.1:c.60235G>C (TTN)	XP_024308862.1:p.Gly20079Arg
XM_024453095.1:c.60232G>C (TTN)	XP_024308863.1:p.Gly20078Arg
XM_024453096.1:c.59665G>C (TTN)	XP_024308864.1:p.Gly19889Arg
XM_024453097.1:c.57007G>C (TTN)	XP_024308865.1:p.Gly19003Arg
XM_024453098.1:c.56926G>C (TTN)	XP_024308866.1:p.Gly18976Arg
XM_024453099.1:c.38689G>C (TTN)	XP_024308867.1:p.Gly12897Arg
XM_024453100.1:c.28543G>C (TTN)	XP_024308868.1:p.Gly9515Arg