Canonical Allele Identifier: CA181959

Gene: TTN

Linked Data

• ClinVar Variation Id: 178264
• ClinVar RCV Id: RCV000155005 ; RCV000713962 ; RCV002516117 ; RCV004544430
• dbSNP Id: rs199565715
• ExAC: 2:179620947 A / G
• gnomAD v2: 2-179620947-A-G
• gnomAD v3: 2-178756220-A-G
• gnomAD v4: 2-178756220-A-G
• MyVariant Identifiers: chr2:g.179620947A>G (hg19) ; chr2:g.178756220A>G (hg38)
• PubMed: PMID:23891399

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178756220A>G , CM000664.2:g.178756220A>G	GRCh38
NC_000002.11:g.179620947A>G , CM000664.1:g.179620947A>G	GRCh37
NC_000002.10:g.179329192A>G	NCBI36
NG_011618.3:g.79583T>C , LRG_391:g.79583T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.10303+2764T>C	ENSP00000343764.6:n.10303+2764T>C
ENST00000342175.11:c.10741+2T>C	ENSP00000340554.6:n.10741+2T>C
ENST00000359218.10:c.10540+1322T>C	ENSP00000352154.5:n.10540+1322T>C
ENST00000360870.10:c.10303+2764T>C MANE Plus Clinical	ENSP00000354117.4:n.10303+2764T>C
ENST00000342175.10:c.10741+2T>C	ENSP00000340554.6:n.10741+2T>C
ENST00000342992.10:c.10303+2764T>C	ENSP00000343764.6:n.10303+2764T>C
ENST00000359218.9:c.10540+1322T>C	ENSP00000352154.5:n.10540+1322T>C
ENST00000360870.9:c.10303+2764T>C	ENSP00000354117.4:n.10303+2764T>C
ENST00000460472.6:c.10165+2764T>C	ENSP00000434586.1:n.10165+2764T>C
ENST00000589042.5:c.11254+2T>C MANE Select	ENSP00000467141.1:n.11254+2T>C
ENST00000591111.5:c.10303+2764T>C	ENSP00000465570.1:n.10303+2764T>C
ENST00000615779.4:c.10303+2764T>C	ENSP00000483597.1:n.10303+2764T>C
ENST00000634225.1:c.900-2211T>C
NM_001256850.1:c.10303+2764T>C	NP_001243779.1:n.10303+2764T>C
NM_001267550.2:c.11254+2T>C MANE Select	NP_001254479.2:n.11254+2T>C
NM_003319.4:c.10165+2764T>C	NP_003310.4:n.10165+2764T>C
NM_133378.4:c.10303+2764T>C	NP_596869.4:n.10303+2764T>C
NM_133379.4:c.10303+2764T>C , LRG_391t2:c.10303+2764T>C	NP_596870.2:n.10303+2764T>C
NM_133432.3:c.10540+1322T>C	NP_597676.3:n.10540+1322T>C
NM_133437.4:c.10741+2T>C	NP_597681.4:n.10741+2T>C
XM_011511729.1:c.10351+2764T>C	XP_011510031.1:n.10351+2764T>C
XM_011511730.1:c.10351+2764T>C	XP_011510032.1:n.10351+2764T>C
XM_011511731.1:c.10210+2764T>C	XP_011510033.1:n.10210+2764T>C
XM_011511732.1:c.10348+2764T>C	XP_011510034.1:n.10348+2764T>C
XM_017004819.1:c.10306+2764T>C	XP_016860308.1:n.10306+2764T>C
XM_017004820.1:c.10306+2764T>C	XP_016860309.1:n.10306+2764T>C
XM_017004821.1:c.10303+2764T>C	XP_016860310.1:n.10303+2764T>C
XM_017004822.1:c.10306+2764T>C	XP_016860311.1:n.10306+2764T>C
XM_017004823.1:c.10306+2764T>C	XP_016860312.1:n.10306+2764T>C
XM_024453094.1:c.10306+2764T>C	XP_024308862.1:n.10306+2764T>C
XM_024453095.1:c.10306+2764T>C	XP_024308863.1:n.10306+2764T>C
XM_024453096.1:c.10306+2764T>C	XP_024308864.1:n.10306+2764T>C
XM_024453097.1:c.10306+2764T>C	XP_024308865.1:n.10306+2764T>C
XM_024453098.1:c.10306+2764T>C	XP_024308866.1:n.10306+2764T>C
XM_024453099.1:c.10306+2764T>C	XP_024308867.1:n.10306+2764T>C
NM_133379.5:c.10303+2764T>C MANE Plus Clinical	NP_596870.2:n.10303+2764T>C