Canonical Allele Identifier: CA349471379

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179411477T>C (hg19) ; chr2:g.178546750T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546750T>C , CM000664.2:g.178546750T>C	GRCh38
NC_000002.11:g.179411477T>C , CM000664.1:g.179411477T>C	GRCh37
NC_000002.10:g.179119723T>C	NCBI36
NG_011618.3:g.289053A>G , LRG_391:g.289053A>G
NG_051363.1:g.28924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86974A>G (TTN)	ENSP00000343764.6:p.Asn28992Asp
ENST00000342175.11:c.68059A>G (TTN)	ENSP00000340554.6:p.Asn22687Asp
ENST00000359218.10:c.67858A>G (TTN)	ENSP00000352154.5:p.Asn22620Asp
ENST00000342175.10:c.68059A>G (TTN)	ENSP00000340554.6:p.Asn22687Asp
ENST00000342992.10:c.86974A>G (TTN)	ENSP00000343764.6:p.Asn28992Asp
ENST00000359218.9:c.67858A>G (TTN)	ENSP00000352154.5:p.Asn22620Asp
ENST00000460472.6:c.67483A>G (TTN)	ENSP00000434586.1:p.Asn22495Asp
ENST00000589042.5:c.94678A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn31560Asp
ENST00000591111.5:c.89755A>G (TTN)	ENSP00000465570.1:p.Asn29919Asp
ENST00000615779.4:c.89755A>G (TTN)	ENSP00000483597.1:p.Asn29919Asp
NM_001256850.1:c.89755A>G (TTN)	NP_001243779.1:p.Asn29919Asp
NM_001267550.2:c.94678A>G (TTN) MANE Select	NP_001254479.2:p.Asn31560Asp
NM_003319.4:c.67483A>G (TTN)	NP_003310.4:p.Asn22495Asp
NM_133378.4:c.86974A>G (TTN)	NP_596869.4:p.Asn28992Asp
NM_133432.3:c.67858A>G (TTN)	NP_597676.3:p.Asn22620Asp
NM_133437.4:c.68059A>G (TTN)	NP_597681.4:p.Asn22687Asp
NR_038271.1:n.446+23114T>C (TTN-AS1)
NR_038272.1:n.2043+4389T>C (TTN-AS1)
XM_011511729.1:c.93775A>G (TTN)	XP_011510031.1:p.Asn31259Asp
XM_011511730.1:c.67669A>G (TTN)	XP_011510032.1:p.Asn22557Asp
XM_011511731.1:c.67528A>G (TTN)	XP_011510033.1:p.Asn22510Asp
XM_017004819.1:c.93571A>G (TTN)	XP_016860308.1:p.Asn31191Asp
XM_017004820.1:c.88969A>G (TTN)	XP_016860309.1:p.Asn29657Asp
XM_017004821.1:c.88966A>G (TTN)	XP_016860310.1:p.Asn29656Asp
XM_017004822.1:c.86008A>G (TTN)	XP_016860311.1:p.Asn28670Asp
XM_017004823.1:c.67624A>G (TTN)	XP_016860312.1:p.Asn22542Asp
XM_024453094.1:c.89119A>G (TTN)	XP_024308862.1:p.Asn29707Asp
XM_024453095.1:c.89116A>G (TTN)	XP_024308863.1:p.Asn29706Asp
XM_024453096.1:c.88549A>G (TTN)	XP_024308864.1:p.Asn29517Asp
XM_024453097.1:c.85891A>G (TTN)	XP_024308865.1:p.Asn28631Asp
XM_024453098.1:c.85810A>G (TTN)	XP_024308866.1:p.Asn28604Asp
XM_024453099.1:c.67573A>G (TTN)	XP_024308867.1:p.Asn22525Asp
XM_024453100.1:c.57427A>G (TTN)	XP_024308868.1:p.Asn19143Asp