Canonical Allele Identifier: CA349405198

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394761T>A (hg19) ; chr2:g.178530034T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530034T>A , CM000664.2:g.178530034T>A	GRCh38
NC_000002.11:g.179394761T>A , CM000664.1:g.179394761T>A	GRCh37
NC_000002.10:g.179103007T>A	NCBI36
NG_011618.3:g.305769A>T , LRG_391:g.305769A>T
NG_051363.1:g.12208T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98753A>T (TTN)	ENSP00000343764.6:p.Asp32918Val
ENST00000342175.11:c.79838A>T (TTN)	ENSP00000340554.6:p.Asp26613Val
ENST00000359218.10:c.79637A>T (TTN)	ENSP00000352154.5:p.Asp26546Val
ENST00000342175.10:c.79838A>T (TTN)	ENSP00000340554.6:p.Asp26613Val
ENST00000342992.10:c.98753A>T (TTN)	ENSP00000343764.6:p.Asp32918Val
ENST00000359218.9:c.79637A>T (TTN)	ENSP00000352154.5:p.Asp26546Val
ENST00000460472.6:c.79262A>T (TTN)	ENSP00000434586.1:p.Asp26421Val
ENST00000589042.5:c.106457A>T (TTN) MANE Select	ENSP00000467141.1:p.Asp35486Val
ENST00000591111.5:c.101534A>T (TTN)	ENSP00000465570.1:p.Asp33845Val
ENST00000615779.4:c.101534A>T (TTN)	ENSP00000483597.1:p.Asp33845Val
NM_001256850.1:c.101534A>T (TTN)	NP_001243779.1:p.Asp33845Val
NM_001267550.2:c.106457A>T (TTN) MANE Select	NP_001254479.2:p.Asp35486Val
NM_003319.4:c.79262A>T (TTN)	NP_003310.4:p.Asp26421Val
NM_133378.4:c.98753A>T (TTN)	NP_596869.4:p.Asp32918Val
NM_133432.3:c.79637A>T (TTN)	NP_597676.3:p.Asp26546Val
NM_133437.4:c.79838A>T (TTN)	NP_597681.4:p.Asp26613Val
NR_038271.1:n.446+6398T>A (TTN-AS1)
NR_038272.1:n.220-5698T>A (TTN-AS1)
XM_011511729.1:c.105554A>T (TTN)	XP_011510031.1:p.Asp35185Val
XM_011511730.1:c.79448A>T (TTN)	XP_011510032.1:p.Asp26483Val
XM_011511731.1:c.79307A>T (TTN)	XP_011510033.1:p.Asp26436Val
XM_017004819.1:c.105350A>T (TTN)	XP_016860308.1:p.Asp35117Val
XM_017004820.1:c.100748A>T (TTN)	XP_016860309.1:p.Asp33583Val
XM_017004821.1:c.100745A>T (TTN)	XP_016860310.1:p.Asp33582Val
XM_017004822.1:c.97787A>T (TTN)	XP_016860311.1:p.Asp32596Val
XM_017004823.1:c.79403A>T (TTN)	XP_016860312.1:p.Asp26468Val
XM_024453094.1:c.100898A>T (TTN)	XP_024308862.1:p.Asp33633Val
XM_024453095.1:c.100895A>T (TTN)	XP_024308863.1:p.Asp33632Val
XM_024453096.1:c.100328A>T (TTN)	XP_024308864.1:p.Asp33443Val
XM_024453097.1:c.97670A>T (TTN)	XP_024308865.1:p.Asp32557Val
XM_024453098.1:c.97589A>T (TTN)	XP_024308866.1:p.Asp32530Val
XM_024453099.1:c.79352A>T (TTN)	XP_024308867.1:p.Asp26451Val
XM_024453100.1:c.69206A>T (TTN)	XP_024308868.1:p.Asp23069Val