Canonical Allele Identifier: CA1310541646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178595676A= , CM000664.2:g.178595676A= GRCh38
NC_000002.11:g.179460403A= , CM000664.1:g.179460403A= GRCh37
NC_000002.10:g.179168649A= NCBI36
NG_011618.3:g.240127T= , LRG_391:g.240127T=
NG_051363.1:g.77850A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.49974T= (TTN) ENSP00000343764.6:p.Ser16658=
ENST00000342175.11:c.31059T= (TTN) ENSP00000340554.6:p.Ser10353=
ENST00000359218.10:c.30858T= (TTN) ENSP00000352154.5:p.Ser10286=
ENST00000342175.10:c.31059T= (TTN) ENSP00000340554.6:p.Ser10353=
ENST00000342992.10:c.49974T= (TTN) ENSP00000343764.6:p.Ser16658=
ENST00000359218.9:c.30858T= (TTN) ENSP00000352154.5:p.Ser10286=
ENST00000460472.6:c.30483T= (TTN) ENSP00000434586.1:p.Ser10161=
ENST00000589042.5:c.57678T= (TTN) MANE Select ENSP00000467141.1:p.Ser19226=
ENST00000591111.5:c.52755T= (TTN) ENSP00000465570.1:p.Ser17585=
ENST00000615779.4:c.52755T= (TTN) ENSP00000483597.1:p.Ser17585=
NM_001256850.1:c.52755T= (TTN) NP_001243779.1:p.Ser17585=
NM_001267550.2:c.57678T= (TTN) MANE Select NP_001254479.2:p.Ser19226=
NM_003319.4:c.30483T= (TTN) NP_003310.4:p.Ser10161=
NM_133378.4:c.49974T= (TTN) NP_596869.4:p.Ser16658=
NM_133432.3:c.30858T= (TTN) NP_597676.3:p.Ser10286=
NM_133437.4:c.31059T= (TTN) NP_597681.4:p.Ser10353=
NR_038271.1:n.597-1920A= (TTN-AS1)
NR_038272.1:n.3365-1920A= (TTN-AS1)
XM_011511729.1:c.56775T= (TTN) XP_011510031.1:p.Ser18925=
XM_011511730.1:c.30669T= (TTN) XP_011510032.1:p.Ser10223=
XM_011511731.1:c.30528T= (TTN) XP_011510033.1:p.Ser10176=
XM_017004819.1:c.56571T= (TTN) XP_016860308.1:p.Ser18857=
XM_017004820.1:c.51969T= (TTN) XP_016860309.1:p.Ser17323=
XM_017004821.1:c.51966T= (TTN) XP_016860310.1:p.Ser17322=
XM_017004822.1:c.49008T= (TTN) XP_016860311.1:p.Ser16336=
XM_017004823.1:c.30624T= (TTN) XP_016860312.1:p.Ser10208=
XM_024453094.1:c.52119T= (TTN) XP_024308862.1:p.Ser17373=
XM_024453095.1:c.52116T= (TTN) XP_024308863.1:p.Ser17372=
XM_024453096.1:c.51549T= (TTN) XP_024308864.1:p.Ser17183=
XM_024453097.1:c.48891T= (TTN) XP_024308865.1:p.Ser16297=
XM_024453098.1:c.48810T= (TTN) XP_024308866.1:p.Ser16270=
XM_024453099.1:c.30573T= (TTN) XP_024308867.1:p.Ser10191=
XM_024453100.1:c.20427T= (TTN) XP_024308868.1:p.Ser6809=