Canonical Allele Identifier: CA349483660

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179455857C>G (hg19) ; chr2:g.178591130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591130C>G , CM000664.2:g.178591130C>G	GRCh38
NC_000002.11:g.179455857C>G , CM000664.1:g.179455857C>G	GRCh37
NC_000002.10:g.179164103C>G	NCBI36
NG_011618.3:g.244673G>C , LRG_391:g.244673G>C
NG_051363.1:g.73304C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52891G>C (TTN)	ENSP00000343764.6:p.Asp17631His
ENST00000342175.11:c.33976G>C (TTN)	ENSP00000340554.6:p.Asp11326His
ENST00000359218.10:c.33775G>C (TTN)	ENSP00000352154.5:p.Asp11259His
ENST00000342175.10:c.33976G>C (TTN)	ENSP00000340554.6:p.Asp11326His
ENST00000342992.10:c.52891G>C (TTN)	ENSP00000343764.6:p.Asp17631His
ENST00000359218.9:c.33775G>C (TTN)	ENSP00000352154.5:p.Asp11259His
ENST00000460472.6:c.33400G>C (TTN)	ENSP00000434586.1:p.Asp11134His
ENST00000589042.5:c.60595G>C (TTN) MANE Select	ENSP00000467141.1:p.Asp20199His
ENST00000591111.5:c.55672G>C (TTN)	ENSP00000465570.1:p.Asp18558His
ENST00000615779.4:c.55672G>C (TTN)	ENSP00000483597.1:p.Asp18558His
NM_001256850.1:c.55672G>C (TTN)	NP_001243779.1:p.Asp18558His
NM_001267550.2:c.60595G>C (TTN) MANE Select	NP_001254479.2:p.Asp20199His
NM_003319.4:c.33400G>C (TTN)	NP_003310.4:p.Asp11134His
NM_133378.4:c.52891G>C (TTN)	NP_596869.4:p.Asp17631His
NM_133432.3:c.33775G>C (TTN)	NP_597676.3:p.Asp11259His
NM_133437.4:c.33976G>C (TTN)	NP_597681.4:p.Asp11326His
NR_038271.1:n.597-6466C>G (TTN-AS1)
NR_038272.1:n.3189-9C>G (TTN-AS1)
XM_011511729.1:c.59692G>C (TTN)	XP_011510031.1:p.Asp19898His
XM_011511730.1:c.33586G>C (TTN)	XP_011510032.1:p.Asp11196His
XM_011511731.1:c.33445G>C (TTN)	XP_011510033.1:p.Asp11149His
XM_017004819.1:c.59488G>C (TTN)	XP_016860308.1:p.Asp19830His
XM_017004820.1:c.54886G>C (TTN)	XP_016860309.1:p.Asp18296His
XM_017004821.1:c.54883G>C (TTN)	XP_016860310.1:p.Asp18295His
XM_017004822.1:c.51925G>C (TTN)	XP_016860311.1:p.Asp17309His
XM_017004823.1:c.33541G>C (TTN)	XP_016860312.1:p.Asp11181His
XM_024453094.1:c.55036G>C (TTN)	XP_024308862.1:p.Asp18346His
XM_024453095.1:c.55033G>C (TTN)	XP_024308863.1:p.Asp18345His
XM_024453096.1:c.54466G>C (TTN)	XP_024308864.1:p.Asp18156His
XM_024453097.1:c.51808G>C (TTN)	XP_024308865.1:p.Asp17270His
XM_024453098.1:c.51727G>C (TTN)	XP_024308866.1:p.Asp17243His
XM_024453099.1:c.33490G>C (TTN)	XP_024308867.1:p.Asp11164His
XM_024453100.1:c.23344G>C (TTN)	XP_024308868.1:p.Asp7782His