Canonical Allele Identifier: CA10605482
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 286486
dbSNP Id: rs886043405

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178729785G>A , CM000664.2:g.178729785G>A GRCh38
NC_000002.11:g.179594512G>A , CM000664.1:g.179594512G>A GRCh37
NC_000002.10:g.179302757G>A NCBI36
NG_011618.3:g.106018C>T , LRG_391:g.106018C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.14736C>T ENSP00000343764.6:p.Phe4912=
ENST00000342175.11:c.13858+8297C>T ENSP00000340554.6:n.13858+8297C>T
ENST00000359218.10:c.13657+8297C>T ENSP00000352154.5:n.13657+8297C>T
ENST00000342175.10:c.13858+8297C>T ENSP00000340554.6:n.13858+8297C>T
ENST00000342992.10:c.14736C>T ENSP00000343764.6:p.Phe4912=
ENST00000359218.9:c.13657+8297C>T ENSP00000352154.5:n.13657+8297C>T
ENST00000460472.6:c.13282+8297C>T ENSP00000434586.1:n.13282+8297C>T
ENST00000589042.5:c.18468C>T MANE Select ENSP00000467141.1:p.Phe6156=
ENST00000591111.5:c.17517C>T ENSP00000465570.1:p.Phe5839=
ENST00000615779.4:c.17517C>T ENSP00000483597.1:p.Phe5839=
NM_001256850.1:c.17517C>T NP_001243779.1:p.Phe5839=
NM_001267550.2:c.18468C>T MANE Select NP_001254479.2:p.Phe6156=
NM_003319.4:c.13282+8297C>T NP_003310.4:n.13282+8297C>T
NM_133378.4:c.14736C>T NP_596869.4:p.Phe4912=
NM_133432.3:c.13657+8297C>T NP_597676.3:n.13657+8297C>T
NM_133437.4:c.13858+8297C>T NP_597681.4:n.13858+8297C>T
XM_011511729.1:c.17565C>T XP_011510031.1:p.Phe5855=
XM_011511730.1:c.13468+8297C>T XP_011510032.1:n.13468+8297C>T
XM_011511731.1:c.13327+8297C>T XP_011510033.1:n.13327+8297C>T
XM_017004819.1:c.17520C>T XP_016860308.1:p.Phe5840=
XM_017004820.1:c.14739C>T XP_016860309.1:p.Phe4913=
XM_017004821.1:c.14736C>T XP_016860310.1:p.Phe4912=
XM_017004822.1:c.17520C>T XP_016860311.1:p.Phe5840=
XM_017004823.1:c.13423+8297C>T XP_016860312.1:n.13423+8297C>T
XM_024453094.1:c.17520C>T XP_024308862.1:p.Phe5840=
XM_024453095.1:c.17520C>T XP_024308863.1:p.Phe5840=
XM_024453096.1:c.17520C>T XP_024308864.1:p.Phe5840=
XM_024453097.1:c.17520C>T XP_024308865.1:p.Phe5840=
XM_024453098.1:c.17520C>T XP_024308866.1:p.Phe5840=
XM_024453099.1:c.13423+8297C>T XP_024308867.1:n.13423+8297C>T