Canonical Allele Identifier: CA349664603

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178575984-A-G
• MyVariant Identifiers: chr2:g.179440711A>G (hg19) ; chr2:g.178575984A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178575984A>G , CM000664.2:g.178575984A>G	GRCh38
NC_000002.11:g.179440711A>G , CM000664.1:g.179440711A>G	GRCh37
NC_000002.10:g.179148957A>G	NCBI36
NG_011618.3:g.259819T>C , LRG_391:g.259819T>C
NG_051363.1:g.58158A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.62444T>C (TTN)	ENSP00000343764.6:p.Ile20815Thr
ENST00000342175.11:c.43529T>C (TTN)	ENSP00000340554.6:p.Ile14510Thr
ENST00000359218.10:c.43328T>C (TTN)	ENSP00000352154.5:p.Ile14443Thr
ENST00000342175.10:c.43529T>C (TTN)	ENSP00000340554.6:p.Ile14510Thr
ENST00000342992.10:c.62444T>C (TTN)	ENSP00000343764.6:p.Ile20815Thr
ENST00000359218.9:c.43328T>C (TTN)	ENSP00000352154.5:p.Ile14443Thr
ENST00000460472.6:c.42953T>C (TTN)	ENSP00000434586.1:p.Ile14318Thr
ENST00000589042.5:c.70148T>C (TTN) MANE Select	ENSP00000467141.1:p.Ile23383Thr
ENST00000591111.5:c.65225T>C (TTN)	ENSP00000465570.1:p.Ile21742Thr
ENST00000615779.4:c.65225T>C (TTN)	ENSP00000483597.1:p.Ile21742Thr
NM_001256850.1:c.65225T>C (TTN)	NP_001243779.1:p.Ile21742Thr
NM_001267550.2:c.70148T>C (TTN) MANE Select	NP_001254479.2:p.Ile23383Thr
NM_003319.4:c.42953T>C (TTN)	NP_003310.4:p.Ile14318Thr
NM_133378.4:c.62444T>C (TTN)	NP_596869.4:p.Ile20815Thr
NM_133432.3:c.43328T>C (TTN)	NP_597676.3:p.Ile14443Thr
NM_133437.4:c.43529T>C (TTN)	NP_597681.4:p.Ile14510Thr
NR_038271.1:n.596+4535A>G (TTN-AS1)
NR_038272.1:n.2044-6588A>G (TTN-AS1)
XM_011511729.1:c.69245T>C (TTN)	XP_011510031.1:p.Ile23082Thr
XM_011511730.1:c.43139T>C (TTN)	XP_011510032.1:p.Ile14380Thr
XM_011511731.1:c.42998T>C (TTN)	XP_011510033.1:p.Ile14333Thr
XM_017004819.1:c.69041T>C (TTN)	XP_016860308.1:p.Ile23014Thr
XM_017004820.1:c.64439T>C (TTN)	XP_016860309.1:p.Ile21480Thr
XM_017004821.1:c.64436T>C (TTN)	XP_016860310.1:p.Ile21479Thr
XM_017004822.1:c.61478T>C (TTN)	XP_016860311.1:p.Ile20493Thr
XM_017004823.1:c.43094T>C (TTN)	XP_016860312.1:p.Ile14365Thr
XM_024453094.1:c.64589T>C (TTN)	XP_024308862.1:p.Ile21530Thr
XM_024453095.1:c.64586T>C (TTN)	XP_024308863.1:p.Ile21529Thr
XM_024453096.1:c.64019T>C (TTN)	XP_024308864.1:p.Ile21340Thr
XM_024453097.1:c.61361T>C (TTN)	XP_024308865.1:p.Ile20454Thr
XM_024453098.1:c.61280T>C (TTN)	XP_024308866.1:p.Ile20427Thr
XM_024453099.1:c.43043T>C (TTN)	XP_024308867.1:p.Ile14348Thr
XM_024453100.1:c.32897T>C (TTN)	XP_024308868.1:p.Ile10966Thr