Canonical Allele Identifier: CA349629615
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178620456C>A , CM000664.2:g.178620456C>A GRCh38
NC_000002.11:g.179485183C>A , CM000664.1:g.179485183C>A GRCh37
NC_000002.10:g.179193428C>A NCBI36
NG_011618.3:g.215347G>T , LRG_391:g.215347G>T
NG_051363.1:g.102630C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.38361G>T ENSP00000343764.6:p.Lys12787Asn
ENST00000342175.11:c.19446G>T ENSP00000340554.6:p.Lys6482Asn
ENST00000359218.10:c.19245G>T ENSP00000352154.5:p.Lys6415Asn
ENST00000342175.10:c.19446G>T ENSP00000340554.6:p.Lys6482Asn
ENST00000342992.10:c.38361G>T ENSP00000343764.6:p.Lys12787Asn
ENST00000359218.9:c.19245G>T ENSP00000352154.5:p.Lys6415Asn
ENST00000460472.6:c.18870G>T ENSP00000434586.1:p.Lys6290Asn
ENST00000589042.5:c.46065G>T MANE Select ENSP00000467141.1:p.Lys15355Asn
ENST00000591111.5:c.41142G>T ENSP00000465570.1:p.Lys13714Asn
ENST00000615779.4:c.41142G>T ENSP00000483597.1:p.Lys13714Asn
NM_001256850.1:c.41142G>T NP_001243779.1:p.Lys13714Asn
NM_001267550.2:c.46065G>T MANE Select NP_001254479.2:p.Lys15355Asn
NM_003319.4:c.18870G>T NP_003310.4:p.Lys6290Asn
NM_133378.4:c.38361G>T NP_596869.4:p.Lys12787Asn
NM_133432.3:c.19245G>T NP_597676.3:p.Lys6415Asn
NM_133437.4:c.19446G>T NP_597681.4:p.Lys6482Asn
XM_011511729.1:c.45162G>T XP_011510031.1:p.Lys15054Asn
XM_011511730.1:c.19056G>T XP_011510032.1:p.Lys6352Asn
XM_011511731.1:c.18915G>T XP_011510033.1:p.Lys6305Asn
XM_017004819.1:c.44958G>T XP_016860308.1:p.Lys14986Asn
XM_017004820.1:c.40356G>T XP_016860309.1:p.Lys13452Asn
XM_017004821.1:c.40353G>T XP_016860310.1:p.Lys13451Asn
XM_017004822.1:c.37395G>T XP_016860311.1:p.Lys12465Asn
XM_017004823.1:c.19011G>T XP_016860312.1:p.Lys6337Asn
XM_024453094.1:c.40506G>T XP_024308862.1:p.Lys13502Asn
XM_024453095.1:c.40503G>T XP_024308863.1:p.Lys13501Asn
XM_024453096.1:c.39936G>T XP_024308864.1:p.Lys13312Asn
XM_024453097.1:c.37278G>T XP_024308865.1:p.Lys12426Asn
XM_024453098.1:c.37197G>T XP_024308866.1:p.Lys12399Asn
XM_024453099.1:c.18960G>T XP_024308867.1:p.Lys6320Asn
XM_024453100.1:c.8814G>T XP_024308868.1:p.Lys2938Asn