Canonical Allele Identifier: CA349645580
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630319T>G , CM000664.2:g.178630319T>G GRCh38
NC_000002.11:g.179495046T>G , CM000664.1:g.179495046T>G GRCh37
NC_000002.10:g.179203291T>G NCBI36
NG_011618.3:g.205484A>C , LRG_391:g.205484A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36499A>C ENSP00000343764.6:p.Asn12167His
ENST00000342175.11:c.17584A>C ENSP00000340554.6:p.Asn5862His
ENST00000359218.10:c.17383A>C ENSP00000352154.5:p.Asn5795His
ENST00000342175.10:c.17584A>C ENSP00000340554.6:p.Asn5862His
ENST00000342992.10:c.36499A>C ENSP00000343764.6:p.Asn12167His
ENST00000359218.9:c.17383A>C ENSP00000352154.5:p.Asn5795His
ENST00000460472.6:c.17008A>C ENSP00000434586.1:p.Asn5670His
ENST00000589042.5:c.44203A>C MANE Select ENSP00000467141.1:p.Asn14735His
ENST00000591111.5:c.39280A>C ENSP00000465570.1:p.Asn13094His
ENST00000615779.4:c.39280A>C ENSP00000483597.1:p.Asn13094His
NM_001256850.1:c.39280A>C NP_001243779.1:p.Asn13094His
NM_001267550.2:c.44203A>C MANE Select NP_001254479.2:p.Asn14735His
NM_003319.4:c.17008A>C NP_003310.4:p.Asn5670His
NM_133378.4:c.36499A>C NP_596869.4:p.Asn12167His
NM_133432.3:c.17383A>C NP_597676.3:p.Asn5795His
NM_133437.4:c.17584A>C NP_597681.4:p.Asn5862His
XM_011511729.1:c.43300A>C XP_011510031.1:p.Asn14434His
XM_011511730.1:c.17194A>C XP_011510032.1:p.Asn5732His
XM_011511731.1:c.17053A>C XP_011510033.1:p.Asn5685His
XM_017004819.1:c.43096A>C XP_016860308.1:p.Asn14366His
XM_017004820.1:c.38494A>C XP_016860309.1:p.Asn12832His
XM_017004821.1:c.38491A>C XP_016860310.1:p.Asn12831His
XM_017004822.1:c.35533A>C XP_016860311.1:p.Asn11845His
XM_017004823.1:c.17149A>C XP_016860312.1:p.Asn5717His
XM_024453094.1:c.38644A>C XP_024308862.1:p.Asn12882His
XM_024453095.1:c.38641A>C XP_024308863.1:p.Asn12881His
XM_024453096.1:c.38074A>C XP_024308864.1:p.Asn12692His
XM_024453097.1:c.35416A>C XP_024308865.1:p.Asn11806His
XM_024453098.1:c.35335A>C XP_024308866.1:p.Asn11779His
XM_024453099.1:c.17098A>C XP_024308867.1:p.Asn5700His
XM_024453100.1:c.6952A>C XP_024308868.1:p.Asn2318His