Canonical Allele Identifier: CA349496165

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414558T>C (hg19) ; chr2:g.178549831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549831T>C , CM000664.2:g.178549831T>C	GRCh38
NC_000002.11:g.179414558T>C , CM000664.1:g.179414558T>C	GRCh37
NC_000002.10:g.179122804T>C	NCBI36
NG_011618.3:g.285972A>G , LRG_391:g.285972A>G
NG_051363.1:g.32005T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84187A>G (TTN)	ENSP00000343764.6:p.Asn28063Asp
ENST00000342175.11:c.65272A>G (TTN)	ENSP00000340554.6:p.Asn21758Asp
ENST00000359218.10:c.65071A>G (TTN)	ENSP00000352154.5:p.Asn21691Asp
ENST00000342175.10:c.65272A>G (TTN)	ENSP00000340554.6:p.Asn21758Asp
ENST00000342992.10:c.84187A>G (TTN)	ENSP00000343764.6:p.Asn28063Asp
ENST00000359218.9:c.65071A>G (TTN)	ENSP00000352154.5:p.Asn21691Asp
ENST00000460472.6:c.64696A>G (TTN)	ENSP00000434586.1:p.Asn21566Asp
ENST00000589042.5:c.91891A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn30631Asp
ENST00000591111.5:c.86968A>G (TTN)	ENSP00000465570.1:p.Asn28990Asp
ENST00000615779.4:c.86968A>G (TTN)	ENSP00000483597.1:p.Asn28990Asp
NM_001256850.1:c.86968A>G (TTN)	NP_001243779.1:p.Asn28990Asp
NM_001267550.2:c.91891A>G (TTN) MANE Select	NP_001254479.2:p.Asn30631Asp
NM_003319.4:c.64696A>G (TTN)	NP_003310.4:p.Asn21566Asp
NM_133378.4:c.84187A>G (TTN)	NP_596869.4:p.Asn28063Asp
NM_133432.3:c.65071A>G (TTN)	NP_597676.3:p.Asn21691Asp
NM_133437.4:c.65272A>G (TTN)	NP_597681.4:p.Asn21758Asp
NR_038271.1:n.447-21469T>C (TTN-AS1)
NR_038272.1:n.2043+7470T>C (TTN-AS1)
XM_011511729.1:c.90988A>G (TTN)	XP_011510031.1:p.Asn30330Asp
XM_011511730.1:c.64882A>G (TTN)	XP_011510032.1:p.Asn21628Asp
XM_011511731.1:c.64741A>G (TTN)	XP_011510033.1:p.Asn21581Asp
XM_017004819.1:c.90784A>G (TTN)	XP_016860308.1:p.Asn30262Asp
XM_017004820.1:c.86182A>G (TTN)	XP_016860309.1:p.Asn28728Asp
XM_017004821.1:c.86179A>G (TTN)	XP_016860310.1:p.Asn28727Asp
XM_017004822.1:c.83221A>G (TTN)	XP_016860311.1:p.Asn27741Asp
XM_017004823.1:c.64837A>G (TTN)	XP_016860312.1:p.Asn21613Asp
XM_024453094.1:c.86332A>G (TTN)	XP_024308862.1:p.Asn28778Asp
XM_024453095.1:c.86329A>G (TTN)	XP_024308863.1:p.Asn28777Asp
XM_024453096.1:c.85762A>G (TTN)	XP_024308864.1:p.Asn28588Asp
XM_024453097.1:c.83104A>G (TTN)	XP_024308865.1:p.Asn27702Asp
XM_024453098.1:c.83023A>G (TTN)	XP_024308866.1:p.Asn27675Asp
XM_024453099.1:c.64786A>G (TTN)	XP_024308867.1:p.Asn21596Asp
XM_024453100.1:c.54640A>G (TTN)	XP_024308868.1:p.Asn18214Asp