Canonical Allele Identifier: CA349645599
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630322G>T , CM000664.2:g.178630322G>T GRCh38
NC_000002.11:g.179495049G>T , CM000664.1:g.179495049G>T GRCh37
NC_000002.10:g.179203294G>T NCBI36
NG_011618.3:g.205481C>A , LRG_391:g.205481C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36496C>A ENSP00000343764.6:p.His12166Asn
ENST00000342175.11:c.17581C>A ENSP00000340554.6:p.His5861Asn
ENST00000359218.10:c.17380C>A ENSP00000352154.5:p.His5794Asn
ENST00000342175.10:c.17581C>A ENSP00000340554.6:p.His5861Asn
ENST00000342992.10:c.36496C>A ENSP00000343764.6:p.His12166Asn
ENST00000359218.9:c.17380C>A ENSP00000352154.5:p.His5794Asn
ENST00000460472.6:c.17005C>A ENSP00000434586.1:p.His5669Asn
ENST00000589042.5:c.44200C>A MANE Select ENSP00000467141.1:p.His14734Asn
ENST00000591111.5:c.39277C>A ENSP00000465570.1:p.His13093Asn
ENST00000615779.4:c.39277C>A ENSP00000483597.1:p.His13093Asn
NM_001256850.1:c.39277C>A NP_001243779.1:p.His13093Asn
NM_001267550.2:c.44200C>A MANE Select NP_001254479.2:p.His14734Asn
NM_003319.4:c.17005C>A NP_003310.4:p.His5669Asn
NM_133378.4:c.36496C>A NP_596869.4:p.His12166Asn
NM_133432.3:c.17380C>A NP_597676.3:p.His5794Asn
NM_133437.4:c.17581C>A NP_597681.4:p.His5861Asn
XM_011511729.1:c.43297C>A XP_011510031.1:p.His14433Asn
XM_011511730.1:c.17191C>A XP_011510032.1:p.His5731Asn
XM_011511731.1:c.17050C>A XP_011510033.1:p.His5684Asn
XM_017004819.1:c.43093C>A XP_016860308.1:p.His14365Asn
XM_017004820.1:c.38491C>A XP_016860309.1:p.His12831Asn
XM_017004821.1:c.38488C>A XP_016860310.1:p.His12830Asn
XM_017004822.1:c.35530C>A XP_016860311.1:p.His11844Asn
XM_017004823.1:c.17146C>A XP_016860312.1:p.His5716Asn
XM_024453094.1:c.38641C>A XP_024308862.1:p.His12881Asn
XM_024453095.1:c.38638C>A XP_024308863.1:p.His12880Asn
XM_024453096.1:c.38071C>A XP_024308864.1:p.His12691Asn
XM_024453097.1:c.35413C>A XP_024308865.1:p.His11805Asn
XM_024453098.1:c.35332C>A XP_024308866.1:p.His11778Asn
XM_024453099.1:c.17095C>A XP_024308867.1:p.His5699Asn
XM_024453100.1:c.6949C>A XP_024308868.1:p.His2317Asn