Canonical Allele Identifier: CA349672070

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179442625T>G (hg19) ; chr2:g.178577898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577898T>G , CM000664.2:g.178577898T>G	GRCh38
NC_000002.11:g.179442625T>G , CM000664.1:g.179442625T>G	GRCh37
NC_000002.10:g.179150871T>G	NCBI36
NG_011618.3:g.257905A>C , LRG_391:g.257905A>C
NG_051363.1:g.60072T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.60824A>C (TTN)	ENSP00000343764.6:p.Asp20275Ala
ENST00000342175.11:c.41909A>C (TTN)	ENSP00000340554.6:p.Asp13970Ala
ENST00000359218.10:c.41708A>C (TTN)	ENSP00000352154.5:p.Asp13903Ala
ENST00000342175.10:c.41909A>C (TTN)	ENSP00000340554.6:p.Asp13970Ala
ENST00000342992.10:c.60824A>C (TTN)	ENSP00000343764.6:p.Asp20275Ala
ENST00000359218.9:c.41708A>C (TTN)	ENSP00000352154.5:p.Asp13903Ala
ENST00000460472.6:c.41333A>C (TTN)	ENSP00000434586.1:p.Asp13778Ala
ENST00000589042.5:c.68528A>C (TTN) MANE Select	ENSP00000467141.1:p.Asp22843Ala
ENST00000591111.5:c.63605A>C (TTN)	ENSP00000465570.1:p.Asp21202Ala
ENST00000615779.4:c.63605A>C (TTN)	ENSP00000483597.1:p.Asp21202Ala
NM_001256850.1:c.63605A>C (TTN)	NP_001243779.1:p.Asp21202Ala
NM_001267550.2:c.68528A>C (TTN) MANE Select	NP_001254479.2:p.Asp22843Ala
NM_003319.4:c.41333A>C (TTN)	NP_003310.4:p.Asp13778Ala
NM_133378.4:c.60824A>C (TTN)	NP_596869.4:p.Asp20275Ala
NM_133432.3:c.41708A>C (TTN)	NP_597676.3:p.Asp13903Ala
NM_133437.4:c.41909A>C (TTN)	NP_597681.4:p.Asp13970Ala
NR_038271.1:n.596+6449T>G (TTN-AS1)
NR_038272.1:n.2044-4674T>G (TTN-AS1)
XM_011511729.1:c.67625A>C (TTN)	XP_011510031.1:p.Asp22542Ala
XM_011511730.1:c.41519A>C (TTN)	XP_011510032.1:p.Asp13840Ala
XM_011511731.1:c.41378A>C (TTN)	XP_011510033.1:p.Asp13793Ala
XM_017004819.1:c.67421A>C (TTN)	XP_016860308.1:p.Asp22474Ala
XM_017004820.1:c.62819A>C (TTN)	XP_016860309.1:p.Asp20940Ala
XM_017004821.1:c.62816A>C (TTN)	XP_016860310.1:p.Asp20939Ala
XM_017004822.1:c.59858A>C (TTN)	XP_016860311.1:p.Asp19953Ala
XM_017004823.1:c.41474A>C (TTN)	XP_016860312.1:p.Asp13825Ala
XM_024453094.1:c.62969A>C (TTN)	XP_024308862.1:p.Asp20990Ala
XM_024453095.1:c.62966A>C (TTN)	XP_024308863.1:p.Asp20989Ala
XM_024453096.1:c.62399A>C (TTN)	XP_024308864.1:p.Asp20800Ala
XM_024453097.1:c.59741A>C (TTN)	XP_024308865.1:p.Asp19914Ala
XM_024453098.1:c.59660A>C (TTN)	XP_024308866.1:p.Asp19887Ala
XM_024453099.1:c.41423A>C (TTN)	XP_024308867.1:p.Asp13808Ala
XM_024453100.1:c.31277A>C (TTN)	XP_024308868.1:p.Asp10426Ala