Canonical Allele Identifier: CA349503440

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179416477A>C (hg19) ; chr2:g.178551750A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551750A>C , CM000664.2:g.178551750A>C	GRCh38
NC_000002.11:g.179416477A>C , CM000664.1:g.179416477A>C	GRCh37
NC_000002.10:g.179124723A>C	NCBI36
NG_011618.3:g.284053T>G , LRG_391:g.284053T>G
NG_051363.1:g.33924A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.83446T>G (TTN)	ENSP00000343764.6:p.Tyr27816Asp
ENST00000342175.11:c.64531T>G (TTN)	ENSP00000340554.6:p.Tyr21511Asp
ENST00000359218.10:c.64330T>G (TTN)	ENSP00000352154.5:p.Tyr21444Asp
ENST00000342175.10:c.64531T>G (TTN)	ENSP00000340554.6:p.Tyr21511Asp
ENST00000342992.10:c.83446T>G (TTN)	ENSP00000343764.6:p.Tyr27816Asp
ENST00000359218.9:c.64330T>G (TTN)	ENSP00000352154.5:p.Tyr21444Asp
ENST00000460472.6:c.63955T>G (TTN)	ENSP00000434586.1:p.Tyr21319Asp
ENST00000589042.5:c.91150T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr30384Asp
ENST00000591111.5:c.86227T>G (TTN)	ENSP00000465570.1:p.Tyr28743Asp
ENST00000615779.4:c.86227T>G (TTN)	ENSP00000483597.1:p.Tyr28743Asp
NM_001256850.1:c.86227T>G (TTN)	NP_001243779.1:p.Tyr28743Asp
NM_001267550.2:c.91150T>G (TTN) MANE Select	NP_001254479.2:p.Tyr30384Asp
NM_003319.4:c.63955T>G (TTN)	NP_003310.4:p.Tyr21319Asp
NM_133378.4:c.83446T>G (TTN)	NP_596869.4:p.Tyr27816Asp
NM_133432.3:c.64330T>G (TTN)	NP_597676.3:p.Tyr21444Asp
NM_133437.4:c.64531T>G (TTN)	NP_597681.4:p.Tyr21511Asp
NR_038271.1:n.447-19550A>C (TTN-AS1)
NR_038272.1:n.2043+9389A>C (TTN-AS1)
XM_011511729.1:c.90247T>G (TTN)	XP_011510031.1:p.Tyr30083Asp
XM_011511730.1:c.64141T>G (TTN)	XP_011510032.1:p.Tyr21381Asp
XM_011511731.1:c.64000T>G (TTN)	XP_011510033.1:p.Tyr21334Asp
XM_017004819.1:c.90043T>G (TTN)	XP_016860308.1:p.Tyr30015Asp
XM_017004820.1:c.85441T>G (TTN)	XP_016860309.1:p.Tyr28481Asp
XM_017004821.1:c.85438T>G (TTN)	XP_016860310.1:p.Tyr28480Asp
XM_017004822.1:c.82480T>G (TTN)	XP_016860311.1:p.Tyr27494Asp
XM_017004823.1:c.64096T>G (TTN)	XP_016860312.1:p.Tyr21366Asp
XM_024453094.1:c.85591T>G (TTN)	XP_024308862.1:p.Tyr28531Asp
XM_024453095.1:c.85588T>G (TTN)	XP_024308863.1:p.Tyr28530Asp
XM_024453096.1:c.85021T>G (TTN)	XP_024308864.1:p.Tyr28341Asp
XM_024453097.1:c.82363T>G (TTN)	XP_024308865.1:p.Tyr27455Asp
XM_024453098.1:c.82282T>G (TTN)	XP_024308866.1:p.Tyr27428Asp
XM_024453099.1:c.64045T>G (TTN)	XP_024308867.1:p.Tyr21349Asp
XM_024453100.1:c.53899T>G (TTN)	XP_024308868.1:p.Tyr17967Asp