Canonical Allele Identifier: CA349457354

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409149T>C (hg19) ; chr2:g.178544422T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544422T>C , CM000664.2:g.178544422T>C	GRCh38
NC_000002.11:g.179409149T>C , CM000664.1:g.179409149T>C	GRCh37
NC_000002.10:g.179117395T>C	NCBI36
NG_011618.3:g.291381A>G , LRG_391:g.291381A>G
NG_051363.1:g.26596T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.88103A>G (TTN)	ENSP00000343764.6:p.Asp29368Gly
ENST00000342175.11:c.69188A>G (TTN)	ENSP00000340554.6:p.Asp23063Gly
ENST00000359218.10:c.68987A>G (TTN)	ENSP00000352154.5:p.Asp22996Gly
ENST00000342175.10:c.69188A>G (TTN)	ENSP00000340554.6:p.Asp23063Gly
ENST00000342992.10:c.88103A>G (TTN)	ENSP00000343764.6:p.Asp29368Gly
ENST00000359218.9:c.68987A>G (TTN)	ENSP00000352154.5:p.Asp22996Gly
ENST00000460472.6:c.68612A>G (TTN)	ENSP00000434586.1:p.Asp22871Gly
ENST00000589042.5:c.95807A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp31936Gly
ENST00000591111.5:c.90884A>G (TTN)	ENSP00000465570.1:p.Asp30295Gly
ENST00000615779.4:c.90884A>G (TTN)	ENSP00000483597.1:p.Asp30295Gly
NM_001256850.1:c.90884A>G (TTN)	NP_001243779.1:p.Asp30295Gly
NM_001267550.2:c.95807A>G (TTN) MANE Select	NP_001254479.2:p.Asp31936Gly
NM_003319.4:c.68612A>G (TTN)	NP_003310.4:p.Asp22871Gly
NM_133378.4:c.88103A>G (TTN)	NP_596869.4:p.Asp29368Gly
NM_133432.3:c.68987A>G (TTN)	NP_597676.3:p.Asp22996Gly
NM_133437.4:c.69188A>G (TTN)	NP_597681.4:p.Asp23063Gly
NR_038271.1:n.446+20786T>C (TTN-AS1)
NR_038272.1:n.2043+2061T>C (TTN-AS1)
XM_011511729.1:c.94904A>G (TTN)	XP_011510031.1:p.Asp31635Gly
XM_011511730.1:c.68798A>G (TTN)	XP_011510032.1:p.Asp22933Gly
XM_011511731.1:c.68657A>G (TTN)	XP_011510033.1:p.Asp22886Gly
XM_017004819.1:c.94700A>G (TTN)	XP_016860308.1:p.Asp31567Gly
XM_017004820.1:c.90098A>G (TTN)	XP_016860309.1:p.Asp30033Gly
XM_017004821.1:c.90095A>G (TTN)	XP_016860310.1:p.Asp30032Gly
XM_017004822.1:c.87137A>G (TTN)	XP_016860311.1:p.Asp29046Gly
XM_017004823.1:c.68753A>G (TTN)	XP_016860312.1:p.Asp22918Gly
XM_024453094.1:c.90248A>G (TTN)	XP_024308862.1:p.Asp30083Gly
XM_024453095.1:c.90245A>G (TTN)	XP_024308863.1:p.Asp30082Gly
XM_024453096.1:c.89678A>G (TTN)	XP_024308864.1:p.Asp29893Gly
XM_024453097.1:c.87020A>G (TTN)	XP_024308865.1:p.Asp29007Gly
XM_024453098.1:c.86939A>G (TTN)	XP_024308866.1:p.Asp28980Gly
XM_024453099.1:c.68702A>G (TTN)	XP_024308867.1:p.Asp22901Gly
XM_024453100.1:c.58556A>G (TTN)	XP_024308868.1:p.Asp19519Gly