Canonical Allele Identifier: CA430260529

Linked Data

MyVariant Identifiers: chr2:g.179444023T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178579296T>C , CM000664.2:g.178579296T>C GRCh38
NC_000002.11:g.179444023T>C , CM000664.1:g.179444023T>C GRCh37
NC_000002.10:g.179152269T>C NCBI36
NG_011618.3:g.256507A>G , LRG_391:g.256507A>G
NG_051363.1:g.61470T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.60030A>G (TTN) ENSP00000343764.6:p.Pro20010=
ENST00000342175.11:c.41115A>G (TTN) ENSP00000340554.6:p.Pro13705=
ENST00000359218.10:c.40914A>G (TTN) ENSP00000352154.5:p.Pro13638=
ENST00000342175.10:c.41115A>G (TTN) ENSP00000340554.6:p.Pro13705=
ENST00000342992.10:c.60030A>G (TTN) ENSP00000343764.6:p.Pro20010=
ENST00000359218.9:c.40914A>G (TTN) ENSP00000352154.5:p.Pro13638=
ENST00000460472.6:c.40539A>G (TTN) ENSP00000434586.1:p.Pro13513=
ENST00000589042.5:c.67734A>G (TTN) MANE Select ENSP00000467141.1:p.Pro22578=
ENST00000591111.5:c.62811A>G (TTN) ENSP00000465570.1:p.Pro20937=
ENST00000615779.4:c.62811A>G (TTN) ENSP00000483597.1:p.Pro20937=
NM_001256850.1:c.62811A>G (TTN) NP_001243779.1:p.Pro20937=
NM_001267550.2:c.67734A>G (TTN) MANE Select NP_001254479.2:p.Pro22578=
NM_003319.4:c.40539A>G (TTN) NP_003310.4:p.Pro13513=
NM_133378.4:c.60030A>G (TTN) NP_596869.4:p.Pro20010=
NM_133432.3:c.40914A>G (TTN) NP_597676.3:p.Pro13638=
NM_133437.4:c.41115A>G (TTN) NP_597681.4:p.Pro13705=
NR_038271.1:n.596+7847T>C (TTN-AS1)
NR_038272.1:n.2044-3276T>C (TTN-AS1)
XM_011511729.1:c.66831A>G (TTN) XP_011510031.1:p.Pro22277=
XM_011511730.1:c.40725A>G (TTN) XP_011510032.1:p.Pro13575=
XM_011511731.1:c.40584A>G (TTN) XP_011510033.1:p.Pro13528=
XM_017004819.1:c.66627A>G (TTN) XP_016860308.1:p.Pro22209=
XM_017004820.1:c.62025A>G (TTN) XP_016860309.1:p.Pro20675=
XM_017004821.1:c.62022A>G (TTN) XP_016860310.1:p.Pro20674=
XM_017004822.1:c.59064A>G (TTN) XP_016860311.1:p.Pro19688=
XM_017004823.1:c.40680A>G (TTN) XP_016860312.1:p.Pro13560=
XM_024453094.1:c.62175A>G (TTN) XP_024308862.1:p.Pro20725=
XM_024453095.1:c.62172A>G (TTN) XP_024308863.1:p.Pro20724=
XM_024453096.1:c.61605A>G (TTN) XP_024308864.1:p.Pro20535=
XM_024453097.1:c.58947A>G (TTN) XP_024308865.1:p.Pro19649=
XM_024453098.1:c.58866A>G (TTN) XP_024308866.1:p.Pro19622=
XM_024453099.1:c.40629A>G (TTN) XP_024308867.1:p.Pro13543=
XM_024453100.1:c.30483A>G (TTN) XP_024308868.1:p.Pro10161=