Canonical Allele Identifier: CA349423339

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179444296T>C (hg19) ; chr2:g.178579569T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178579569T>C , CM000664.2:g.178579569T>C	GRCh38
NC_000002.11:g.179444296T>C , CM000664.1:g.179444296T>C	GRCh37
NC_000002.10:g.179152542T>C	NCBI36
NG_011618.3:g.256234A>G , LRG_391:g.256234A>G
NG_051363.1:g.61743T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.59924A>G (TTN)	ENSP00000343764.6:p.Asp19975Gly
ENST00000342175.11:c.41009A>G (TTN)	ENSP00000340554.6:p.Asp13670Gly
ENST00000359218.10:c.40808A>G (TTN)	ENSP00000352154.5:p.Asp13603Gly
ENST00000342175.10:c.41009A>G (TTN)	ENSP00000340554.6:p.Asp13670Gly
ENST00000342992.10:c.59924A>G (TTN)	ENSP00000343764.6:p.Asp19975Gly
ENST00000359218.9:c.40808A>G (TTN)	ENSP00000352154.5:p.Asp13603Gly
ENST00000460472.6:c.40433A>G (TTN)	ENSP00000434586.1:p.Asp13478Gly
ENST00000589042.5:c.67628A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp22543Gly
ENST00000591111.5:c.62705A>G (TTN)	ENSP00000465570.1:p.Asp20902Gly
ENST00000615779.4:c.62705A>G (TTN)	ENSP00000483597.1:p.Asp20902Gly
NM_001256850.1:c.62705A>G (TTN)	NP_001243779.1:p.Asp20902Gly
NM_001267550.2:c.67628A>G (TTN) MANE Select	NP_001254479.2:p.Asp22543Gly
NM_003319.4:c.40433A>G (TTN)	NP_003310.4:p.Asp13478Gly
NM_133378.4:c.59924A>G (TTN)	NP_596869.4:p.Asp19975Gly
NM_133432.3:c.40808A>G (TTN)	NP_597676.3:p.Asp13603Gly
NM_133437.4:c.41009A>G (TTN)	NP_597681.4:p.Asp13670Gly
NR_038271.1:n.596+8120T>C (TTN-AS1)
NR_038272.1:n.2044-3003T>C (TTN-AS1)
XM_011511729.1:c.66725A>G (TTN)	XP_011510031.1:p.Asp22242Gly
XM_011511730.1:c.40619A>G (TTN)	XP_011510032.1:p.Asp13540Gly
XM_011511731.1:c.40478A>G (TTN)	XP_011510033.1:p.Asp13493Gly
XM_017004819.1:c.66521A>G (TTN)	XP_016860308.1:p.Asp22174Gly
XM_017004820.1:c.61919A>G (TTN)	XP_016860309.1:p.Asp20640Gly
XM_017004821.1:c.61916A>G (TTN)	XP_016860310.1:p.Asp20639Gly
XM_017004822.1:c.58958A>G (TTN)	XP_016860311.1:p.Asp19653Gly
XM_017004823.1:c.40574A>G (TTN)	XP_016860312.1:p.Asp13525Gly
XM_024453094.1:c.62069A>G (TTN)	XP_024308862.1:p.Asp20690Gly
XM_024453095.1:c.62066A>G (TTN)	XP_024308863.1:p.Asp20689Gly
XM_024453096.1:c.61499A>G (TTN)	XP_024308864.1:p.Asp20500Gly
XM_024453097.1:c.58841A>G (TTN)	XP_024308865.1:p.Asp19614Gly
XM_024453098.1:c.58760A>G (TTN)	XP_024308866.1:p.Asp19587Gly
XM_024453099.1:c.40523A>G (TTN)	XP_024308867.1:p.Asp13508Gly
XM_024453100.1:c.30377A>G (TTN)	XP_024308868.1:p.Asp10126Gly