Canonical Allele Identifier: CA349434770

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179404681T>C (hg19) ; chr2:g.178539954T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539954T>C , CM000664.2:g.178539954T>C	GRCh38
NC_000002.11:g.179404681T>C , CM000664.1:g.179404681T>C	GRCh37
NC_000002.10:g.179112927T>C	NCBI36
NG_011618.3:g.295849A>G , LRG_391:g.295849A>G
NG_051363.1:g.22128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.90407A>G (TTN)	ENSP00000343764.6:p.Tyr30136Cys
ENST00000342175.11:c.71492A>G (TTN)	ENSP00000340554.6:p.Tyr23831Cys
ENST00000359218.10:c.71291A>G (TTN)	ENSP00000352154.5:p.Tyr23764Cys
ENST00000342175.10:c.71492A>G (TTN)	ENSP00000340554.6:p.Tyr23831Cys
ENST00000342992.10:c.90407A>G (TTN)	ENSP00000343764.6:p.Tyr30136Cys
ENST00000359218.9:c.71291A>G (TTN)	ENSP00000352154.5:p.Tyr23764Cys
ENST00000460472.6:c.70916A>G (TTN)	ENSP00000434586.1:p.Tyr23639Cys
ENST00000589042.5:c.98111A>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr32704Cys
ENST00000591111.5:c.93188A>G (TTN)	ENSP00000465570.1:p.Tyr31063Cys
ENST00000615779.4:c.93188A>G (TTN)	ENSP00000483597.1:p.Tyr31063Cys
NM_001256850.1:c.93188A>G (TTN)	NP_001243779.1:p.Tyr31063Cys
NM_001267550.2:c.98111A>G (TTN) MANE Select	NP_001254479.2:p.Tyr32704Cys
NM_003319.4:c.70916A>G (TTN)	NP_003310.4:p.Tyr23639Cys
NM_133378.4:c.90407A>G (TTN)	NP_596869.4:p.Tyr30136Cys
NM_133432.3:c.71291A>G (TTN)	NP_597676.3:p.Tyr23764Cys
NM_133437.4:c.71492A>G (TTN)	NP_597681.4:p.Tyr23831Cys
NR_038271.1:n.446+16318T>C (TTN-AS1)
NR_038272.1:n.1840+64T>C (TTN-AS1)
XM_011511729.1:c.97208A>G (TTN)	XP_011510031.1:p.Tyr32403Cys
XM_011511730.1:c.71102A>G (TTN)	XP_011510032.1:p.Tyr23701Cys
XM_011511731.1:c.70961A>G (TTN)	XP_011510033.1:p.Tyr23654Cys
XM_017004819.1:c.97004A>G (TTN)	XP_016860308.1:p.Tyr32335Cys
XM_017004820.1:c.92402A>G (TTN)	XP_016860309.1:p.Tyr30801Cys
XM_017004821.1:c.92399A>G (TTN)	XP_016860310.1:p.Tyr30800Cys
XM_017004822.1:c.89441A>G (TTN)	XP_016860311.1:p.Tyr29814Cys
XM_017004823.1:c.71057A>G (TTN)	XP_016860312.1:p.Tyr23686Cys
XM_024453094.1:c.92552A>G (TTN)	XP_024308862.1:p.Tyr30851Cys
XM_024453095.1:c.92549A>G (TTN)	XP_024308863.1:p.Tyr30850Cys
XM_024453096.1:c.91982A>G (TTN)	XP_024308864.1:p.Tyr30661Cys
XM_024453097.1:c.89324A>G (TTN)	XP_024308865.1:p.Tyr29775Cys
XM_024453098.1:c.89243A>G (TTN)	XP_024308866.1:p.Tyr29748Cys
XM_024453099.1:c.71006A>G (TTN)	XP_024308867.1:p.Tyr23669Cys
XM_024453100.1:c.60860A>G (TTN)	XP_024308868.1:p.Tyr20287Cys