Canonical Allele Identifier: CA60988311

Gene: TTN

Linked Data

• dbSNP Id: rs1034296192
• gnomAD v2: 2-179554376-AGT-A
• gnomAD v3: 2-178689649-AGT-A
• gnomAD v4: 2-178689649-AGT-A
• MyVariant Identifiers: chr2:g.179554377_179554378del (hg19) ; chr2:g.178689650_178689651del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689650_178689651del , CM000664.2:g.178689650_178689651del	GRCh38
NC_000002.11:g.179554377_179554378del , CM000664.1:g.179554377_179554378del	GRCh37
NC_000002.10:g.179262622_179262623del	NCBI36
NG_011618.3:g.146152_146153del , LRG_391:g.146152_146153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.28115-56_28115-55del	ENSP00000343764.6:n.28115-56_28115-55del
ENST00000342175.11:c.13859-47334_13859-47333del	ENSP00000340554.6:n.13859-47334_13859-47333del
ENST00000359218.10:c.13658-47334_13658-47333del	ENSP00000352154.5:n.13658-47334_13658-47333del
ENST00000342175.10:c.13859-47334_13859-47333del	ENSP00000340554.6:n.13859-47334_13859-47333del
ENST00000342992.10:c.28115-56_28115-55del	ENSP00000343764.6:n.28115-56_28115-55del
ENST00000359218.9:c.13658-47334_13658-47333del	ENSP00000352154.5:n.13658-47334_13658-47333del
ENST00000414766.5:c.1481-56_1481-55del	ENSP00000401501.1:n.1481-56_1481-55del
ENST00000460472.6:c.13283-47334_13283-47333del	ENSP00000434586.1:n.13283-47334_13283-47333del
ENST00000589042.5:c.31847-56_31847-55del MANE Select	ENSP00000467141.1:n.31847-56_31847-55del
ENST00000591111.5:c.30896-56_30896-55del	ENSP00000465570.1:n.30896-56_30896-55del
ENST00000615779.4:c.30896-56_30896-55del	ENSP00000483597.1:n.30896-56_30896-55del
NM_001256850.1:c.30896-56_30896-55del	NP_001243779.1:n.30896-56_30896-55del
NM_001267550.2:c.31847-56_31847-55del MANE Select	NP_001254479.2:n.31847-56_31847-55del
NM_003319.4:c.13283-47334_13283-47333del	NP_003310.4:n.13283-47334_13283-47333del
NM_133378.4:c.28115-56_28115-55del	NP_596869.4:n.28115-56_28115-55del
NM_133432.3:c.13658-47334_13658-47333del	NP_597676.3:n.13658-47334_13658-47333del
NM_133437.4:c.13859-47334_13859-47333del	NP_597681.4:n.13859-47334_13859-47333del
XM_011511729.1:c.30944-56_30944-55del	XP_011510031.1:n.30944-56_30944-55del
XM_011511730.1:c.13469-47334_13469-47333del	XP_011510032.1:n.13469-47334_13469-47333del
XM_011511731.1:c.13328-47334_13328-47333del	XP_011510033.1:n.13328-47334_13328-47333del
XM_017004819.1:c.30899-56_30899-55del	XP_016860308.1:n.30899-56_30899-55del
XM_017004820.1:c.28118-56_28118-55del	XP_016860309.1:n.28118-56_28118-55del
XM_017004821.1:c.28115-56_28115-55del	XP_016860310.1:n.28115-56_28115-55del
XM_017004822.1:c.30899-56_30899-55del	XP_016860311.1:n.30899-56_30899-55del
XM_017004823.1:c.13424-47334_13424-47333del	XP_016860312.1:n.13424-47334_13424-47333del
XM_024453094.1:c.30899-56_30899-55del	XP_024308862.1:n.30899-56_30899-55del
XM_024453095.1:c.30899-56_30899-55del	XP_024308863.1:n.30899-56_30899-55del
XM_024453096.1:c.30899-56_30899-55del	XP_024308864.1:n.30899-56_30899-55del
XM_024453097.1:c.30898+162_30898+163del	XP_024308865.1:n.30898+162_30898+163del
XM_024453098.1:c.30898+162_30898+163del	XP_024308866.1:n.30898+162_30898+163del
XM_024453099.1:c.13424-47334_13424-47333del	XP_024308867.1:n.13424-47334_13424-47333del