Canonical Allele Identifier: CA349512635

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179417392G>C (hg19) ; chr2:g.178552665G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552665G>C , CM000664.2:g.178552665G>C	GRCh38
NC_000002.11:g.179417392G>C , CM000664.1:g.179417392G>C	GRCh37
NC_000002.10:g.179125638G>C	NCBI36
NG_011618.3:g.283138C>G , LRG_391:g.283138C>G
NG_051363.1:g.34839G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82531C>G (TTN)	ENSP00000343764.6:p.His27511Asp
ENST00000342175.11:c.63616C>G (TTN)	ENSP00000340554.6:p.His21206Asp
ENST00000359218.10:c.63415C>G (TTN)	ENSP00000352154.5:p.His21139Asp
ENST00000342175.10:c.63616C>G (TTN)	ENSP00000340554.6:p.His21206Asp
ENST00000342992.10:c.82531C>G (TTN)	ENSP00000343764.6:p.His27511Asp
ENST00000359218.9:c.63415C>G (TTN)	ENSP00000352154.5:p.His21139Asp
ENST00000460472.6:c.63040C>G (TTN)	ENSP00000434586.1:p.His21014Asp
ENST00000589042.5:c.90235C>G (TTN) MANE Select	ENSP00000467141.1:p.His30079Asp
ENST00000591111.5:c.85312C>G (TTN)	ENSP00000465570.1:p.His28438Asp
ENST00000615779.4:c.85312C>G (TTN)	ENSP00000483597.1:p.His28438Asp
NM_001256850.1:c.85312C>G (TTN)	NP_001243779.1:p.His28438Asp
NM_001267550.2:c.90235C>G (TTN) MANE Select	NP_001254479.2:p.His30079Asp
NM_003319.4:c.63040C>G (TTN)	NP_003310.4:p.His21014Asp
NM_133378.4:c.82531C>G (TTN)	NP_596869.4:p.His27511Asp
NM_133432.3:c.63415C>G (TTN)	NP_597676.3:p.His21139Asp
NM_133437.4:c.63616C>G (TTN)	NP_597681.4:p.His21206Asp
NR_038271.1:n.447-18635G>C (TTN-AS1)
NR_038272.1:n.2043+10304G>C (TTN-AS1)
XM_011511729.1:c.89332C>G (TTN)	XP_011510031.1:p.His29778Asp
XM_011511730.1:c.63226C>G (TTN)	XP_011510032.1:p.His21076Asp
XM_011511731.1:c.63085C>G (TTN)	XP_011510033.1:p.His21029Asp
XM_017004819.1:c.89128C>G (TTN)	XP_016860308.1:p.His29710Asp
XM_017004820.1:c.84526C>G (TTN)	XP_016860309.1:p.His28176Asp
XM_017004821.1:c.84523C>G (TTN)	XP_016860310.1:p.His28175Asp
XM_017004822.1:c.81565C>G (TTN)	XP_016860311.1:p.His27189Asp
XM_017004823.1:c.63181C>G (TTN)	XP_016860312.1:p.His21061Asp
XM_024453094.1:c.84676C>G (TTN)	XP_024308862.1:p.His28226Asp
XM_024453095.1:c.84673C>G (TTN)	XP_024308863.1:p.His28225Asp
XM_024453096.1:c.84106C>G (TTN)	XP_024308864.1:p.His28036Asp
XM_024453097.1:c.81448C>G (TTN)	XP_024308865.1:p.His27150Asp
XM_024453098.1:c.81367C>G (TTN)	XP_024308866.1:p.His27123Asp
XM_024453099.1:c.63130C>G (TTN)	XP_024308867.1:p.His21044Asp
XM_024453100.1:c.52984C>G (TTN)	XP_024308868.1:p.His17662Asp