Canonical Allele Identifier: CA349451174
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178712347T>A , CM000664.2:g.178712347T>A GRCh38
NC_000002.11:g.179577074T>A , CM000664.1:g.179577074T>A GRCh37
NC_000002.10:g.179285319T>A NCBI36
NG_011618.3:g.123456A>T , LRG_391:g.123456A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.23843A>T ENSP00000343764.6:p.Lys7948Ile
ENST00000342175.11:c.13858+25735A>T ENSP00000340554.6:n.13858+25735A>T
ENST00000359218.10:c.13657+25735A>T ENSP00000352154.5:n.13657+25735A>T
ENST00000342175.10:c.13858+25735A>T ENSP00000340554.6:n.13858+25735A>T
ENST00000342992.10:c.23843A>T ENSP00000343764.6:p.Lys7948Ile
ENST00000359218.9:c.13657+25735A>T ENSP00000352154.5:n.13657+25735A>T
ENST00000460472.6:c.13282+25735A>T ENSP00000434586.1:n.13282+25735A>T
ENST00000589042.5:c.27575A>T MANE Select ENSP00000467141.1:p.Lys9192Ile
ENST00000591111.5:c.26624A>T ENSP00000465570.1:p.Lys8875Ile
ENST00000615779.4:c.26624A>T ENSP00000483597.1:p.Lys8875Ile
NM_001256850.1:c.26624A>T NP_001243779.1:p.Lys8875Ile
NM_001267550.2:c.27575A>T MANE Select NP_001254479.2:p.Lys9192Ile
NM_003319.4:c.13282+25735A>T NP_003310.4:n.13282+25735A>T
NM_133378.4:c.23843A>T NP_596869.4:p.Lys7948Ile
NM_133432.3:c.13657+25735A>T NP_597676.3:n.13657+25735A>T
NM_133437.4:c.13858+25735A>T NP_597681.4:n.13858+25735A>T
XM_011511729.1:c.26672A>T XP_011510031.1:p.Lys8891Ile
XM_011511730.1:c.13468+25735A>T XP_011510032.1:n.13468+25735A>T
XM_011511731.1:c.13327+25735A>T XP_011510033.1:n.13327+25735A>T
XM_017004819.1:c.26627A>T XP_016860308.1:p.Lys8876Ile
XM_017004820.1:c.23846A>T XP_016860309.1:p.Lys7949Ile
XM_017004821.1:c.23843A>T XP_016860310.1:p.Lys7948Ile
XM_017004822.1:c.26627A>T XP_016860311.1:p.Lys8876Ile
XM_017004823.1:c.13423+25735A>T XP_016860312.1:n.13423+25735A>T
XM_024453094.1:c.26627A>T XP_024308862.1:p.Lys8876Ile
XM_024453095.1:c.26627A>T XP_024308863.1:p.Lys8876Ile
XM_024453096.1:c.26627A>T XP_024308864.1:p.Lys8876Ile
XM_024453097.1:c.26627A>T XP_024308865.1:p.Lys8876Ile
XM_024453098.1:c.26627A>T XP_024308866.1:p.Lys8876Ile
XM_024453099.1:c.13423+25735A>T XP_024308867.1:n.13423+25735A>T