Canonical Allele Identifier: CA349611309

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179433551T>C (hg19) ; chr2:g.178568824T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568824T>C , CM000664.2:g.178568824T>C	GRCh38
NC_000002.11:g.179433551T>C , CM000664.1:g.179433551T>C	GRCh37
NC_000002.10:g.179141797T>C	NCBI36
NG_011618.3:g.266979A>G , LRG_391:g.266979A>G
NG_051363.1:g.50998T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.69604A>G (TTN)	ENSP00000343764.6:p.Arg23202Gly
ENST00000342175.11:c.50689A>G (TTN)	ENSP00000340554.6:p.Arg16897Gly
ENST00000359218.10:c.50488A>G (TTN)	ENSP00000352154.5:p.Arg16830Gly
ENST00000342175.10:c.50689A>G (TTN)	ENSP00000340554.6:p.Arg16897Gly
ENST00000342992.10:c.69604A>G (TTN)	ENSP00000343764.6:p.Arg23202Gly
ENST00000359218.9:c.50488A>G (TTN)	ENSP00000352154.5:p.Arg16830Gly
ENST00000460472.6:c.50113A>G (TTN)	ENSP00000434586.1:p.Arg16705Gly
ENST00000589042.5:c.77308A>G (TTN) MANE Select	ENSP00000467141.1:p.Arg25770Gly
ENST00000591111.5:c.72385A>G (TTN)	ENSP00000465570.1:p.Arg24129Gly
ENST00000615779.4:c.72385A>G (TTN)	ENSP00000483597.1:p.Arg24129Gly
NM_001256850.1:c.72385A>G (TTN)	NP_001243779.1:p.Arg24129Gly
NM_001267550.2:c.77308A>G (TTN) MANE Select	NP_001254479.2:p.Arg25770Gly
NM_003319.4:c.50113A>G (TTN)	NP_003310.4:p.Arg16705Gly
NM_133378.4:c.69604A>G (TTN)	NP_596869.4:p.Arg23202Gly
NM_133432.3:c.50488A>G (TTN)	NP_597676.3:p.Arg16830Gly
NM_133437.4:c.50689A>G (TTN)	NP_597681.4:p.Arg16897Gly
NR_038271.1:n.447-2476T>C (TTN-AS1)
NR_038272.1:n.2044-13748T>C (TTN-AS1)
XM_011511729.1:c.76405A>G (TTN)	XP_011510031.1:p.Arg25469Gly
XM_011511730.1:c.50299A>G (TTN)	XP_011510032.1:p.Arg16767Gly
XM_011511731.1:c.50158A>G (TTN)	XP_011510033.1:p.Arg16720Gly
XM_017004819.1:c.76201A>G (TTN)	XP_016860308.1:p.Arg25401Gly
XM_017004820.1:c.71599A>G (TTN)	XP_016860309.1:p.Arg23867Gly
XM_017004821.1:c.71596A>G (TTN)	XP_016860310.1:p.Arg23866Gly
XM_017004822.1:c.68638A>G (TTN)	XP_016860311.1:p.Arg22880Gly
XM_017004823.1:c.50254A>G (TTN)	XP_016860312.1:p.Arg16752Gly
XM_024453094.1:c.71749A>G (TTN)	XP_024308862.1:p.Arg23917Gly
XM_024453095.1:c.71746A>G (TTN)	XP_024308863.1:p.Arg23916Gly
XM_024453096.1:c.71179A>G (TTN)	XP_024308864.1:p.Arg23727Gly
XM_024453097.1:c.68521A>G (TTN)	XP_024308865.1:p.Arg22841Gly
XM_024453098.1:c.68440A>G (TTN)	XP_024308866.1:p.Arg22814Gly
XM_024453099.1:c.50203A>G (TTN)	XP_024308867.1:p.Arg16735Gly
XM_024453100.1:c.40057A>G (TTN)	XP_024308868.1:p.Arg13353Gly