Canonical Allele Identifier: CA349434774

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179404682A>C (hg19) ; chr2:g.178539955A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539955A>C , CM000664.2:g.178539955A>C	GRCh38
NC_000002.11:g.179404682A>C , CM000664.1:g.179404682A>C	GRCh37
NC_000002.10:g.179112928A>C	NCBI36
NG_011618.3:g.295848T>G , LRG_391:g.295848T>G
NG_051363.1:g.22129A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.90406T>G (TTN)	ENSP00000343764.6:p.Tyr30136Asp
ENST00000342175.11:c.71491T>G (TTN)	ENSP00000340554.6:p.Tyr23831Asp
ENST00000359218.10:c.71290T>G (TTN)	ENSP00000352154.5:p.Tyr23764Asp
ENST00000342175.10:c.71491T>G (TTN)	ENSP00000340554.6:p.Tyr23831Asp
ENST00000342992.10:c.90406T>G (TTN)	ENSP00000343764.6:p.Tyr30136Asp
ENST00000359218.9:c.71290T>G (TTN)	ENSP00000352154.5:p.Tyr23764Asp
ENST00000460472.6:c.70915T>G (TTN)	ENSP00000434586.1:p.Tyr23639Asp
ENST00000589042.5:c.98110T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr32704Asp
ENST00000591111.5:c.93187T>G (TTN)	ENSP00000465570.1:p.Tyr31063Asp
ENST00000615779.4:c.93187T>G (TTN)	ENSP00000483597.1:p.Tyr31063Asp
NM_001256850.1:c.93187T>G (TTN)	NP_001243779.1:p.Tyr31063Asp
NM_001267550.2:c.98110T>G (TTN) MANE Select	NP_001254479.2:p.Tyr32704Asp
NM_003319.4:c.70915T>G (TTN)	NP_003310.4:p.Tyr23639Asp
NM_133378.4:c.90406T>G (TTN)	NP_596869.4:p.Tyr30136Asp
NM_133432.3:c.71290T>G (TTN)	NP_597676.3:p.Tyr23764Asp
NM_133437.4:c.71491T>G (TTN)	NP_597681.4:p.Tyr23831Asp
NR_038271.1:n.446+16319A>C (TTN-AS1)
NR_038272.1:n.1840+65A>C (TTN-AS1)
XM_011511729.1:c.97207T>G (TTN)	XP_011510031.1:p.Tyr32403Asp
XM_011511730.1:c.71101T>G (TTN)	XP_011510032.1:p.Tyr23701Asp
XM_011511731.1:c.70960T>G (TTN)	XP_011510033.1:p.Tyr23654Asp
XM_017004819.1:c.97003T>G (TTN)	XP_016860308.1:p.Tyr32335Asp
XM_017004820.1:c.92401T>G (TTN)	XP_016860309.1:p.Tyr30801Asp
XM_017004821.1:c.92398T>G (TTN)	XP_016860310.1:p.Tyr30800Asp
XM_017004822.1:c.89440T>G (TTN)	XP_016860311.1:p.Tyr29814Asp
XM_017004823.1:c.71056T>G (TTN)	XP_016860312.1:p.Tyr23686Asp
XM_024453094.1:c.92551T>G (TTN)	XP_024308862.1:p.Tyr30851Asp
XM_024453095.1:c.92548T>G (TTN)	XP_024308863.1:p.Tyr30850Asp
XM_024453096.1:c.91981T>G (TTN)	XP_024308864.1:p.Tyr30661Asp
XM_024453097.1:c.89323T>G (TTN)	XP_024308865.1:p.Tyr29775Asp
XM_024453098.1:c.89242T>G (TTN)	XP_024308866.1:p.Tyr29748Asp
XM_024453099.1:c.71005T>G (TTN)	XP_024308867.1:p.Tyr23669Asp
XM_024453100.1:c.60859T>G (TTN)	XP_024308868.1:p.Tyr20287Asp