Canonical Allele Identifier: CA430296080
Gene: TTN HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.179605210C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740483C>A , CM000664.2:g.178740483C>A GRCh38
NC_000002.11:g.179605210C>A , CM000664.1:g.179605210C>A GRCh37
NC_000002.10:g.179313455C>A NCBI36
NG_011618.3:g.95320G>T , LRG_391:g.95320G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2123G>T ENSP00000343764.6:n.10361-2123G>T
ENST00000342175.11:c.12237G>T ENSP00000340554.6:p.Val4079=
ENST00000359218.10:c.12036G>T ENSP00000352154.5:p.Val4012=
ENST00000342175.10:c.12237G>T ENSP00000340554.6:p.Val4079=
ENST00000342992.10:c.10361-2123G>T ENSP00000343764.6:n.10361-2123G>T
ENST00000359218.9:c.12036G>T ENSP00000352154.5:p.Val4012=
ENST00000460472.6:c.11661G>T ENSP00000434586.1:p.Val3887=
ENST00000589042.5:c.12750G>T MANE Select ENSP00000467141.1:p.Val4250=
ENST00000591111.5:c.11799G>T ENSP00000465570.1:p.Val3933=
ENST00000615779.4:c.11799G>T ENSP00000483597.1:p.Val3933=
NM_001256850.1:c.11799G>T NP_001243779.1:p.Val3933=
NM_001267550.2:c.12750G>T MANE Select NP_001254479.2:p.Val4250=
NM_003319.4:c.11661G>T NP_003310.4:p.Val3887=
NM_133378.4:c.10361-2123G>T NP_596869.4:n.10361-2123G>T
NM_133432.3:c.12036G>T NP_597676.3:p.Val4012=
NM_133437.4:c.12237G>T NP_597681.4:p.Val4079=
XM_011511729.1:c.11847G>T XP_011510031.1:p.Val3949=
XM_011511730.1:c.11847G>T XP_011510032.1:p.Val3949=
XM_011511731.1:c.11706G>T XP_011510033.1:p.Val3902=
XM_017004819.1:c.11802G>T XP_016860308.1:p.Val3934=
XM_017004820.1:c.10364-2123G>T XP_016860309.1:n.10364-2123G>T
XM_017004821.1:c.10361-2123G>T XP_016860310.1:n.10361-2123G>T
XM_017004822.1:c.11802G>T XP_016860311.1:p.Val3934=
XM_017004823.1:c.11802G>T XP_016860312.1:p.Val3934=
XM_024453094.1:c.11802G>T XP_024308862.1:p.Val3934=
XM_024453095.1:c.11802G>T XP_024308863.1:p.Val3934=
XM_024453096.1:c.11802G>T XP_024308864.1:p.Val3934=
XM_024453097.1:c.11802G>T XP_024308865.1:p.Val3934=
XM_024453098.1:c.11802G>T XP_024308866.1:p.Val3934=
XM_024453099.1:c.11802G>T XP_024308867.1:p.Val3934=