Canonical Allele Identifier: CA349406732

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395159A>G (hg19) ; chr2:g.178530432A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530432A>G , CM000664.2:g.178530432A>G	GRCh38
NC_000002.11:g.179395159A>G , CM000664.1:g.179395159A>G	GRCh37
NC_000002.10:g.179103405A>G	NCBI36
NG_011618.3:g.305371T>C , LRG_391:g.305371T>C
NG_051363.1:g.12606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98479T>C (TTN)	ENSP00000343764.6:p.Ser32827Pro
ENST00000342175.11:c.79564T>C (TTN)	ENSP00000340554.6:p.Ser26522Pro
ENST00000359218.10:c.79363T>C (TTN)	ENSP00000352154.5:p.Ser26455Pro
ENST00000342175.10:c.79564T>C (TTN)	ENSP00000340554.6:p.Ser26522Pro
ENST00000342992.10:c.98479T>C (TTN)	ENSP00000343764.6:p.Ser32827Pro
ENST00000359218.9:c.79363T>C (TTN)	ENSP00000352154.5:p.Ser26455Pro
ENST00000460472.6:c.78988T>C (TTN)	ENSP00000434586.1:p.Ser26330Pro
ENST00000589042.5:c.106183T>C (TTN) MANE Select	ENSP00000467141.1:p.Ser35395Pro
ENST00000591111.5:c.101260T>C (TTN)	ENSP00000465570.1:p.Ser33754Pro
ENST00000615779.4:c.101260T>C (TTN)	ENSP00000483597.1:p.Ser33754Pro
NM_001256850.1:c.101260T>C (TTN)	NP_001243779.1:p.Ser33754Pro
NM_001267550.2:c.106183T>C (TTN) MANE Select	NP_001254479.2:p.Ser35395Pro
NM_003319.4:c.78988T>C (TTN)	NP_003310.4:p.Ser26330Pro
NM_133378.4:c.98479T>C (TTN)	NP_596869.4:p.Ser32827Pro
NM_133432.3:c.79363T>C (TTN)	NP_597676.3:p.Ser26455Pro
NM_133437.4:c.79564T>C (TTN)	NP_597681.4:p.Ser26522Pro
NR_038271.1:n.446+6796A>G (TTN-AS1)
NR_038272.1:n.220-5300A>G (TTN-AS1)
XM_011511729.1:c.105280T>C (TTN)	XP_011510031.1:p.Ser35094Pro
XM_011511730.1:c.79174T>C (TTN)	XP_011510032.1:p.Ser26392Pro
XM_011511731.1:c.79033T>C (TTN)	XP_011510033.1:p.Ser26345Pro
XM_017004819.1:c.105076T>C (TTN)	XP_016860308.1:p.Ser35026Pro
XM_017004820.1:c.100474T>C (TTN)	XP_016860309.1:p.Ser33492Pro
XM_017004821.1:c.100471T>C (TTN)	XP_016860310.1:p.Ser33491Pro
XM_017004822.1:c.97513T>C (TTN)	XP_016860311.1:p.Ser32505Pro
XM_017004823.1:c.79129T>C (TTN)	XP_016860312.1:p.Ser26377Pro
XM_024453094.1:c.100624T>C (TTN)	XP_024308862.1:p.Ser33542Pro
XM_024453095.1:c.100621T>C (TTN)	XP_024308863.1:p.Ser33541Pro
XM_024453096.1:c.100054T>C (TTN)	XP_024308864.1:p.Ser33352Pro
XM_024453097.1:c.97396T>C (TTN)	XP_024308865.1:p.Ser32466Pro
XM_024453098.1:c.97315T>C (TTN)	XP_024308866.1:p.Ser32439Pro
XM_024453099.1:c.79078T>C (TTN)	XP_024308867.1:p.Ser26360Pro
XM_024453100.1:c.68932T>C (TTN)	XP_024308868.1:p.Ser22978Pro