Canonical Allele Identifier: CA349610569
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740481G>T , CM000664.2:g.178740481G>T GRCh38
NC_000002.11:g.179605208G>T , CM000664.1:g.179605208G>T GRCh37
NC_000002.10:g.179313453G>T NCBI36
NG_011618.3:g.95322C>A , LRG_391:g.95322C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2121C>A ENSP00000343764.6:n.10361-2121C>A
ENST00000342175.11:c.12239C>A ENSP00000340554.6:p.Thr4080Asn
ENST00000359218.10:c.12038C>A ENSP00000352154.5:p.Thr4013Asn
ENST00000342175.10:c.12239C>A ENSP00000340554.6:p.Thr4080Asn
ENST00000342992.10:c.10361-2121C>A ENSP00000343764.6:n.10361-2121C>A
ENST00000359218.9:c.12038C>A ENSP00000352154.5:p.Thr4013Asn
ENST00000460472.6:c.11663C>A ENSP00000434586.1:p.Thr3888Asn
ENST00000589042.5:c.12752C>A MANE Select ENSP00000467141.1:p.Thr4251Asn
ENST00000591111.5:c.11801C>A ENSP00000465570.1:p.Thr3934Asn
ENST00000615779.4:c.11801C>A ENSP00000483597.1:p.Thr3934Asn
NM_001256850.1:c.11801C>A NP_001243779.1:p.Thr3934Asn
NM_001267550.2:c.12752C>A MANE Select NP_001254479.2:p.Thr4251Asn
NM_003319.4:c.11663C>A NP_003310.4:p.Thr3888Asn
NM_133378.4:c.10361-2121C>A NP_596869.4:n.10361-2121C>A
NM_133432.3:c.12038C>A NP_597676.3:p.Thr4013Asn
NM_133437.4:c.12239C>A NP_597681.4:p.Thr4080Asn
XM_011511729.1:c.11849C>A XP_011510031.1:p.Thr3950Asn
XM_011511730.1:c.11849C>A XP_011510032.1:p.Thr3950Asn
XM_011511731.1:c.11708C>A XP_011510033.1:p.Thr3903Asn
XM_017004819.1:c.11804C>A XP_016860308.1:p.Thr3935Asn
XM_017004820.1:c.10364-2121C>A XP_016860309.1:n.10364-2121C>A
XM_017004821.1:c.10361-2121C>A XP_016860310.1:n.10361-2121C>A
XM_017004822.1:c.11804C>A XP_016860311.1:p.Thr3935Asn
XM_017004823.1:c.11804C>A XP_016860312.1:p.Thr3935Asn
XM_024453094.1:c.11804C>A XP_024308862.1:p.Thr3935Asn
XM_024453095.1:c.11804C>A XP_024308863.1:p.Thr3935Asn
XM_024453096.1:c.11804C>A XP_024308864.1:p.Thr3935Asn
XM_024453097.1:c.11804C>A XP_024308865.1:p.Thr3935Asn
XM_024453098.1:c.11804C>A XP_024308866.1:p.Thr3935Asn
XM_024453099.1:c.11804C>A XP_024308867.1:p.Thr3935Asn