Canonical Allele Identifier: CA1310555927
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630318T= , CM000664.2:g.178630318T= GRCh38
NC_000002.11:g.179495045T= , CM000664.1:g.179495045T= GRCh37
NC_000002.10:g.179203290T= NCBI36
NG_011618.3:g.205485A= , LRG_391:g.205485A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36500A= ENSP00000343764.6:p.Asn12167=
ENST00000342175.11:c.17585A= ENSP00000340554.6:p.Asn5862=
ENST00000359218.10:c.17384A= ENSP00000352154.5:p.Asn5795=
ENST00000342175.10:c.17585A= ENSP00000340554.6:p.Asn5862=
ENST00000342992.10:c.36500A= ENSP00000343764.6:p.Asn12167=
ENST00000359218.9:c.17384A= ENSP00000352154.5:p.Asn5795=
ENST00000460472.6:c.17009A= ENSP00000434586.1:p.Asn5670=
ENST00000589042.5:c.44204A= MANE Select ENSP00000467141.1:p.Asn14735=
ENST00000591111.5:c.39281A= ENSP00000465570.1:p.Asn13094=
ENST00000615779.4:c.39281A= ENSP00000483597.1:p.Asn13094=
NM_001256850.1:c.39281A= NP_001243779.1:p.Asn13094=
NM_001267550.2:c.44204A= MANE Select NP_001254479.2:p.Asn14735=
NM_003319.4:c.17009A= NP_003310.4:p.Asn5670=
NM_133378.4:c.36500A= NP_596869.4:p.Asn12167=
NM_133432.3:c.17384A= NP_597676.3:p.Asn5795=
NM_133437.4:c.17585A= NP_597681.4:p.Asn5862=
XM_011511729.1:c.43301A= XP_011510031.1:p.Asn14434=
XM_011511730.1:c.17195A= XP_011510032.1:p.Asn5732=
XM_011511731.1:c.17054A= XP_011510033.1:p.Asn5685=
XM_017004819.1:c.43097A= XP_016860308.1:p.Asn14366=
XM_017004820.1:c.38495A= XP_016860309.1:p.Asn12832=
XM_017004821.1:c.38492A= XP_016860310.1:p.Asn12831=
XM_017004822.1:c.35534A= XP_016860311.1:p.Asn11845=
XM_017004823.1:c.17150A= XP_016860312.1:p.Asn5717=
XM_024453094.1:c.38645A= XP_024308862.1:p.Asn12882=
XM_024453095.1:c.38642A= XP_024308863.1:p.Asn12881=
XM_024453096.1:c.38075A= XP_024308864.1:p.Asn12692=
XM_024453097.1:c.35417A= XP_024308865.1:p.Asn11806=
XM_024453098.1:c.35336A= XP_024308866.1:p.Asn11779=
XM_024453099.1:c.17099A= XP_024308867.1:p.Asn5700=
XM_024453100.1:c.6953A= XP_024308868.1:p.Asn2318=