Canonical Allele Identifier: CA349614331

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179434151T>C (hg19) ; chr2:g.178569424T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569424T>C , CM000664.2:g.178569424T>C	GRCh38
NC_000002.11:g.179434151T>C , CM000664.1:g.179434151T>C	GRCh37
NC_000002.10:g.179142397T>C	NCBI36
NG_011618.3:g.266379A>G , LRG_391:g.266379A>G
NG_051363.1:g.51598T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.69004A>G (TTN)	ENSP00000343764.6:p.Asn23002Asp
ENST00000342175.11:c.50089A>G (TTN)	ENSP00000340554.6:p.Asn16697Asp
ENST00000359218.10:c.49888A>G (TTN)	ENSP00000352154.5:p.Asn16630Asp
ENST00000342175.10:c.50089A>G (TTN)	ENSP00000340554.6:p.Asn16697Asp
ENST00000342992.10:c.69004A>G (TTN)	ENSP00000343764.6:p.Asn23002Asp
ENST00000359218.9:c.49888A>G (TTN)	ENSP00000352154.5:p.Asn16630Asp
ENST00000460472.6:c.49513A>G (TTN)	ENSP00000434586.1:p.Asn16505Asp
ENST00000589042.5:c.76708A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn25570Asp
ENST00000591111.5:c.71785A>G (TTN)	ENSP00000465570.1:p.Asn23929Asp
ENST00000615779.4:c.71785A>G (TTN)	ENSP00000483597.1:p.Asn23929Asp
NM_001256850.1:c.71785A>G (TTN)	NP_001243779.1:p.Asn23929Asp
NM_001267550.2:c.76708A>G (TTN) MANE Select	NP_001254479.2:p.Asn25570Asp
NM_003319.4:c.49513A>G (TTN)	NP_003310.4:p.Asn16505Asp
NM_133378.4:c.69004A>G (TTN)	NP_596869.4:p.Asn23002Asp
NM_133432.3:c.49888A>G (TTN)	NP_597676.3:p.Asn16630Asp
NM_133437.4:c.50089A>G (TTN)	NP_597681.4:p.Asn16697Asp
NR_038271.1:n.447-1876T>C (TTN-AS1)
NR_038272.1:n.2044-13148T>C (TTN-AS1)
XM_011511729.1:c.75805A>G (TTN)	XP_011510031.1:p.Asn25269Asp
XM_011511730.1:c.49699A>G (TTN)	XP_011510032.1:p.Asn16567Asp
XM_011511731.1:c.49558A>G (TTN)	XP_011510033.1:p.Asn16520Asp
XM_017004819.1:c.75601A>G (TTN)	XP_016860308.1:p.Asn25201Asp
XM_017004820.1:c.70999A>G (TTN)	XP_016860309.1:p.Asn23667Asp
XM_017004821.1:c.70996A>G (TTN)	XP_016860310.1:p.Asn23666Asp
XM_017004822.1:c.68038A>G (TTN)	XP_016860311.1:p.Asn22680Asp
XM_017004823.1:c.49654A>G (TTN)	XP_016860312.1:p.Asn16552Asp
XM_024453094.1:c.71149A>G (TTN)	XP_024308862.1:p.Asn23717Asp
XM_024453095.1:c.71146A>G (TTN)	XP_024308863.1:p.Asn23716Asp
XM_024453096.1:c.70579A>G (TTN)	XP_024308864.1:p.Asn23527Asp
XM_024453097.1:c.67921A>G (TTN)	XP_024308865.1:p.Asn22641Asp
XM_024453098.1:c.67840A>G (TTN)	XP_024308866.1:p.Asn22614Asp
XM_024453099.1:c.49603A>G (TTN)	XP_024308867.1:p.Asn16535Asp
XM_024453100.1:c.39457A>G (TTN)	XP_024308868.1:p.Asn13153Asp