Canonical Allele Identifier: CA1996880

Gene: TTN

Linked Data

• ClinVar Variation Id: 467104
• ClinVar RCV Id: RCV000536838 ; RCV000594353 ; RCV000852866
• dbSNP Id: rs763845436
• ExAC: 2:179517256 G / A
• gnomAD v2: 2-179517256-G-A
• gnomAD v3: 2-178652529-G-A
• gnomAD v4: 2-178652529-G-A
• COSMIC: COSM4634677 ; COSM4634678
• MyVariant Identifiers: chr2:g.179517256G>A (hg19) ; chr2:g.178652529G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178652529G>A , CM000664.2:g.178652529G>A	GRCh38
NC_000002.11:g.179517256G>A , CM000664.1:g.179517256G>A	GRCh37
NC_000002.10:g.179225501G>A	NCBI36
NG_011618.3:g.183274C>T , LRG_391:g.183274C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.31754C>T	ENSP00000343764.6:p.Pro10585Leu
ENST00000342175.11:c.13859-10212C>T	ENSP00000340554.6:n.13859-10212C>T
ENST00000359218.10:c.13658-10212C>T	ENSP00000352154.5:n.13658-10212C>T
ENST00000342175.10:c.13859-10212C>T	ENSP00000340554.6:n.13859-10212C>T
ENST00000342992.10:c.31754C>T	ENSP00000343764.6:p.Pro10585Leu
ENST00000359218.9:c.13658-10212C>T	ENSP00000352154.5:n.13658-10212C>T
ENST00000414766.5:c.2441-10212C>T	ENSP00000401501.1:n.2441-10212C>T
ENST00000460472.6:c.13283-10212C>T	ENSP00000434586.1:n.13283-10212C>T
ENST00000589042.5:c.39056C>T MANE Select	ENSP00000467141.1:p.Pro13019Leu
ENST00000591111.5:c.34535C>T	ENSP00000465570.1:p.Pro11512Leu
ENST00000615779.4:c.34535C>T	ENSP00000483597.1:p.Pro11512Leu
NM_001256850.1:c.34535C>T	NP_001243779.1:p.Pro11512Leu
NM_001267550.2:c.39056C>T MANE Select	NP_001254479.2:p.Pro13019Leu
NM_003319.4:c.13283-10212C>T	NP_003310.4:n.13283-10212C>T
NM_133378.4:c.31754C>T	NP_596869.4:p.Pro10585Leu
NM_133432.3:c.13658-10212C>T	NP_597676.3:n.13658-10212C>T
NM_133437.4:c.13859-10212C>T	NP_597681.4:n.13859-10212C>T
XM_011511729.1:c.38153C>T	XP_011510031.1:p.Pro12718Leu
XM_011511730.1:c.13469-10212C>T	XP_011510032.1:n.13469-10212C>T
XM_011511731.1:c.13328-10212C>T	XP_011510033.1:n.13328-10212C>T
XM_017004819.1:c.37949C>T	XP_016860308.1:p.Pro12650Leu
XM_017004820.1:c.33347C>T	XP_016860309.1:p.Pro11116Leu
XM_017004821.1:c.33344C>T	XP_016860310.1:p.Pro11115Leu
XM_017004822.1:c.31859-10212C>T	XP_016860311.1:n.31859-10212C>T
XM_017004823.1:c.13424-10212C>T	XP_016860312.1:n.13424-10212C>T
XM_024453094.1:c.33569-182C>T	XP_024308862.1:n.33569-182C>T
XM_024453095.1:c.33566-182C>T	XP_024308863.1:n.33566-182C>T
XM_024453096.1:c.32999-182C>T	XP_024308864.1:n.32999-182C>T
XM_024453097.1:c.31691-10212C>T	XP_024308865.1:n.31691-10212C>T
XM_024453098.1:c.31610-10212C>T	XP_024308866.1:n.31610-10212C>T
XM_024453099.1:c.13424-10212C>T	XP_024308867.1:n.13424-10212C>T
XM_024453100.1:c.1805C>T	XP_024308868.1:p.Pro602Leu