Canonical Allele Identifier: CA349646962
Gene: TTN HGNC NCBI

Linked Data

dbSNP Id: rs1438118192

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631159T>C , CM000664.2:g.178631159T>C GRCh38
NC_000002.11:g.179495886T>C , CM000664.1:g.179495886T>C GRCh37
NC_000002.10:g.179204131T>C NCBI36
NG_011618.3:g.204644A>G , LRG_391:g.204644A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36185A>G ENSP00000343764.6:p.Asn12062Ser
ENST00000342175.11:c.17270A>G ENSP00000340554.6:p.Asn5757Ser
ENST00000359218.10:c.17069A>G ENSP00000352154.5:p.Asn5690Ser
ENST00000342175.10:c.17270A>G ENSP00000340554.6:p.Asn5757Ser
ENST00000342992.10:c.36185A>G ENSP00000343764.6:p.Asn12062Ser
ENST00000359218.9:c.17069A>G ENSP00000352154.5:p.Asn5690Ser
ENST00000460472.6:c.16694A>G ENSP00000434586.1:p.Asn5565Ser
ENST00000589042.5:c.43889A>G MANE Select ENSP00000467141.1:p.Asn14630Ser
ENST00000591111.5:c.38966A>G ENSP00000465570.1:p.Asn12989Ser
ENST00000615779.4:c.38966A>G ENSP00000483597.1:p.Asn12989Ser
NM_001256850.1:c.38966A>G NP_001243779.1:p.Asn12989Ser
NM_001267550.2:c.43889A>G MANE Select NP_001254479.2:p.Asn14630Ser
NM_003319.4:c.16694A>G NP_003310.4:p.Asn5565Ser
NM_133378.4:c.36185A>G NP_596869.4:p.Asn12062Ser
NM_133432.3:c.17069A>G NP_597676.3:p.Asn5690Ser
NM_133437.4:c.17270A>G NP_597681.4:p.Asn5757Ser
XM_011511729.1:c.42986A>G XP_011510031.1:p.Asn14329Ser
XM_011511730.1:c.16880A>G XP_011510032.1:p.Asn5627Ser
XM_011511731.1:c.16739A>G XP_011510033.1:p.Asn5580Ser
XM_017004819.1:c.42782A>G XP_016860308.1:p.Asn14261Ser
XM_017004820.1:c.38180A>G XP_016860309.1:p.Asn12727Ser
XM_017004821.1:c.38177A>G XP_016860310.1:p.Asn12726Ser
XM_017004822.1:c.35219A>G XP_016860311.1:p.Asn11740Ser
XM_017004823.1:c.16835A>G XP_016860312.1:p.Asn5612Ser
XM_024453094.1:c.38330A>G XP_024308862.1:p.Asn12777Ser
XM_024453095.1:c.38327A>G XP_024308863.1:p.Asn12776Ser
XM_024453096.1:c.37760A>G XP_024308864.1:p.Asn12587Ser
XM_024453097.1:c.35102A>G XP_024308865.1:p.Asn11701Ser
XM_024453098.1:c.35021A>G XP_024308866.1:p.Asn11674Ser
XM_024453099.1:c.16784A>G XP_024308867.1:p.Asn5595Ser
XM_024453100.1:c.6638A>G XP_024308868.1:p.Asn2213Ser