Canonical Allele Identifier: CA349647010
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631170C>G , CM000664.2:g.178631170C>G GRCh38
NC_000002.11:g.179495897C>G , CM000664.1:g.179495897C>G GRCh37
NC_000002.10:g.179204142C>G NCBI36
NG_011618.3:g.204633G>C , LRG_391:g.204633G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36174G>C ENSP00000343764.6:p.Lys12058Asn
ENST00000342175.11:c.17259G>C ENSP00000340554.6:p.Lys5753Asn
ENST00000359218.10:c.17058G>C ENSP00000352154.5:p.Lys5686Asn
ENST00000342175.10:c.17259G>C ENSP00000340554.6:p.Lys5753Asn
ENST00000342992.10:c.36174G>C ENSP00000343764.6:p.Lys12058Asn
ENST00000359218.9:c.17058G>C ENSP00000352154.5:p.Lys5686Asn
ENST00000460472.6:c.16683G>C ENSP00000434586.1:p.Lys5561Asn
ENST00000589042.5:c.43878G>C MANE Select ENSP00000467141.1:p.Lys14626Asn
ENST00000591111.5:c.38955G>C ENSP00000465570.1:p.Lys12985Asn
ENST00000615779.4:c.38955G>C ENSP00000483597.1:p.Lys12985Asn
NM_001256850.1:c.38955G>C NP_001243779.1:p.Lys12985Asn
NM_001267550.2:c.43878G>C MANE Select NP_001254479.2:p.Lys14626Asn
NM_003319.4:c.16683G>C NP_003310.4:p.Lys5561Asn
NM_133378.4:c.36174G>C NP_596869.4:p.Lys12058Asn
NM_133432.3:c.17058G>C NP_597676.3:p.Lys5686Asn
NM_133437.4:c.17259G>C NP_597681.4:p.Lys5753Asn
XM_011511729.1:c.42975G>C XP_011510031.1:p.Lys14325Asn
XM_011511730.1:c.16869G>C XP_011510032.1:p.Lys5623Asn
XM_011511731.1:c.16728G>C XP_011510033.1:p.Lys5576Asn
XM_017004819.1:c.42771G>C XP_016860308.1:p.Lys14257Asn
XM_017004820.1:c.38169G>C XP_016860309.1:p.Lys12723Asn
XM_017004821.1:c.38166G>C XP_016860310.1:p.Lys12722Asn
XM_017004822.1:c.35208G>C XP_016860311.1:p.Lys11736Asn
XM_017004823.1:c.16824G>C XP_016860312.1:p.Lys5608Asn
XM_024453094.1:c.38319G>C XP_024308862.1:p.Lys12773Asn
XM_024453095.1:c.38316G>C XP_024308863.1:p.Lys12772Asn
XM_024453096.1:c.37749G>C XP_024308864.1:p.Lys12583Asn
XM_024453097.1:c.35091G>C XP_024308865.1:p.Lys11697Asn
XM_024453098.1:c.35010G>C XP_024308866.1:p.Lys11670Asn
XM_024453099.1:c.16773G>C XP_024308867.1:p.Lys5591Asn
XM_024453100.1:c.6627G>C XP_024308868.1:p.Lys2209Asn