Canonical Allele Identifier: CA349435408

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179449198A>C (hg19) ; chr2:g.178584471A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584471A>C , CM000664.2:g.178584471A>C	GRCh38
NC_000002.11:g.179449198A>C , CM000664.1:g.179449198A>C	GRCh37
NC_000002.10:g.179157444A>C	NCBI36
NG_011618.3:g.251332T>G , LRG_391:g.251332T>G
NG_051363.1:g.66645A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57376T>G (TTN)	ENSP00000343764.6:p.Tyr19126Asp
ENST00000342175.11:c.38461T>G (TTN)	ENSP00000340554.6:p.Tyr12821Asp
ENST00000359218.10:c.38260T>G (TTN)	ENSP00000352154.5:p.Tyr12754Asp
ENST00000342175.10:c.38461T>G (TTN)	ENSP00000340554.6:p.Tyr12821Asp
ENST00000342992.10:c.57376T>G (TTN)	ENSP00000343764.6:p.Tyr19126Asp
ENST00000359218.9:c.38260T>G (TTN)	ENSP00000352154.5:p.Tyr12754Asp
ENST00000460472.6:c.37885T>G (TTN)	ENSP00000434586.1:p.Tyr12629Asp
ENST00000589042.5:c.65080T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr21694Asp
ENST00000591111.5:c.60157T>G (TTN)	ENSP00000465570.1:p.Tyr20053Asp
ENST00000615779.4:c.60157T>G (TTN)	ENSP00000483597.1:p.Tyr20053Asp
NM_001256850.1:c.60157T>G (TTN)	NP_001243779.1:p.Tyr20053Asp
NM_001267550.2:c.65080T>G (TTN) MANE Select	NP_001254479.2:p.Tyr21694Asp
NM_003319.4:c.37885T>G (TTN)	NP_003310.4:p.Tyr12629Asp
NM_133378.4:c.57376T>G (TTN)	NP_596869.4:p.Tyr19126Asp
NM_133432.3:c.38260T>G (TTN)	NP_597676.3:p.Tyr12754Asp
NM_133437.4:c.38461T>G (TTN)	NP_597681.4:p.Tyr12821Asp
NR_038271.1:n.596+13022A>C (TTN-AS1)
NR_038272.1:n.2768-102A>C (TTN-AS1)
XM_011511729.1:c.64177T>G (TTN)	XP_011510031.1:p.Tyr21393Asp
XM_011511730.1:c.38071T>G (TTN)	XP_011510032.1:p.Tyr12691Asp
XM_011511731.1:c.37930T>G (TTN)	XP_011510033.1:p.Tyr12644Asp
XM_017004819.1:c.63973T>G (TTN)	XP_016860308.1:p.Tyr21325Asp
XM_017004820.1:c.59371T>G (TTN)	XP_016860309.1:p.Tyr19791Asp
XM_017004821.1:c.59368T>G (TTN)	XP_016860310.1:p.Tyr19790Asp
XM_017004822.1:c.56410T>G (TTN)	XP_016860311.1:p.Tyr18804Asp
XM_017004823.1:c.38026T>G (TTN)	XP_016860312.1:p.Tyr12676Asp
XM_024453094.1:c.59521T>G (TTN)	XP_024308862.1:p.Tyr19841Asp
XM_024453095.1:c.59518T>G (TTN)	XP_024308863.1:p.Tyr19840Asp
XM_024453096.1:c.58951T>G (TTN)	XP_024308864.1:p.Tyr19651Asp
XM_024453097.1:c.56293T>G (TTN)	XP_024308865.1:p.Tyr18765Asp
XM_024453098.1:c.56212T>G (TTN)	XP_024308866.1:p.Tyr18738Asp
XM_024453099.1:c.37975T>G (TTN)	XP_024308867.1:p.Tyr12659Asp
XM_024453100.1:c.27829T>G (TTN)	XP_024308868.1:p.Tyr9277Asp