Canonical Allele Identifier: CA2002681
Gene: TTN HGNC NCBI

Linked Data

dbSNP Id: rs763277411

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740581T>C , CM000664.2:g.178740581T>C GRCh38
NC_000002.11:g.179605308T>C , CM000664.1:g.179605308T>C GRCh37
NC_000002.10:g.179313553T>C NCBI36
NG_011618.3:g.95222A>G , LRG_391:g.95222A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2221A>G ENSP00000343764.6:n.10361-2221A>G
ENST00000342175.11:c.12139A>G ENSP00000340554.6:p.Ile4047Val
ENST00000359218.10:c.11938A>G ENSP00000352154.5:p.Ile3980Val
ENST00000342175.10:c.12139A>G ENSP00000340554.6:p.Ile4047Val
ENST00000342992.10:c.10361-2221A>G ENSP00000343764.6:n.10361-2221A>G
ENST00000359218.9:c.11938A>G ENSP00000352154.5:p.Ile3980Val
ENST00000460472.6:c.11563A>G ENSP00000434586.1:p.Ile3855Val
ENST00000589042.5:c.12652A>G MANE Select ENSP00000467141.1:p.Ile4218Val
ENST00000591111.5:c.11701A>G ENSP00000465570.1:p.Ile3901Val
ENST00000615779.4:c.11701A>G ENSP00000483597.1:p.Ile3901Val
NM_001256850.1:c.11701A>G NP_001243779.1:p.Ile3901Val
NM_001267550.2:c.12652A>G MANE Select NP_001254479.2:p.Ile4218Val
NM_003319.4:c.11563A>G NP_003310.4:p.Ile3855Val
NM_133378.4:c.10361-2221A>G NP_596869.4:n.10361-2221A>G
NM_133432.3:c.11938A>G NP_597676.3:p.Ile3980Val
NM_133437.4:c.12139A>G NP_597681.4:p.Ile4047Val
XM_011511729.1:c.11749A>G XP_011510031.1:p.Ile3917Val
XM_011511730.1:c.11749A>G XP_011510032.1:p.Ile3917Val
XM_011511731.1:c.11608A>G XP_011510033.1:p.Ile3870Val
XM_017004819.1:c.11704A>G XP_016860308.1:p.Ile3902Val
XM_017004820.1:c.10364-2221A>G XP_016860309.1:n.10364-2221A>G
XM_017004821.1:c.10361-2221A>G XP_016860310.1:n.10361-2221A>G
XM_017004822.1:c.11704A>G XP_016860311.1:p.Ile3902Val
XM_017004823.1:c.11704A>G XP_016860312.1:p.Ile3902Val
XM_024453094.1:c.11704A>G XP_024308862.1:p.Ile3902Val
XM_024453095.1:c.11704A>G XP_024308863.1:p.Ile3902Val
XM_024453096.1:c.11704A>G XP_024308864.1:p.Ile3902Val
XM_024453097.1:c.11704A>G XP_024308865.1:p.Ile3902Val
XM_024453098.1:c.11704A>G XP_024308866.1:p.Ile3902Val
XM_024453099.1:c.11704A>G XP_024308867.1:p.Ile3902Val