Canonical Allele Identifier: CA1310521143

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178551680A= , CM000664.2:g.178551680A= GRCh38
NC_000002.11:g.179416407A= , CM000664.1:g.179416407A= GRCh37
NC_000002.10:g.179124653A= NCBI36
NG_011618.3:g.284123T= , LRG_391:g.284123T=
NG_051363.1:g.33854A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.83516T= (TTN) ENSP00000343764.6:p.Leu27839=
ENST00000342175.11:c.64601T= (TTN) ENSP00000340554.6:p.Leu21534=
ENST00000359218.10:c.64400T= (TTN) ENSP00000352154.5:p.Leu21467=
ENST00000342175.10:c.64601T= (TTN) ENSP00000340554.6:p.Leu21534=
ENST00000342992.10:c.83516T= (TTN) ENSP00000343764.6:p.Leu27839=
ENST00000359218.9:c.64400T= (TTN) ENSP00000352154.5:p.Leu21467=
ENST00000460472.6:c.64025T= (TTN) ENSP00000434586.1:p.Leu21342=
ENST00000589042.5:c.91220T= (TTN) MANE Select ENSP00000467141.1:p.Leu30407=
ENST00000591111.5:c.86297T= (TTN) ENSP00000465570.1:p.Leu28766=
ENST00000615779.4:c.86297T= (TTN) ENSP00000483597.1:p.Leu28766=
NM_001256850.1:c.86297T= (TTN) NP_001243779.1:p.Leu28766=
NM_001267550.2:c.91220T= (TTN) MANE Select NP_001254479.2:p.Leu30407=
NM_003319.4:c.64025T= (TTN) NP_003310.4:p.Leu21342=
NM_133378.4:c.83516T= (TTN) NP_596869.4:p.Leu27839=
NM_133432.3:c.64400T= (TTN) NP_597676.3:p.Leu21467=
NM_133437.4:c.64601T= (TTN) NP_597681.4:p.Leu21534=
NR_038271.1:n.447-19620A= (TTN-AS1)
NR_038272.1:n.2043+9319A= (TTN-AS1)
XM_011511729.1:c.90317T= (TTN) XP_011510031.1:p.Leu30106=
XM_011511730.1:c.64211T= (TTN) XP_011510032.1:p.Leu21404=
XM_011511731.1:c.64070T= (TTN) XP_011510033.1:p.Leu21357=
XM_017004819.1:c.90113T= (TTN) XP_016860308.1:p.Leu30038=
XM_017004820.1:c.85511T= (TTN) XP_016860309.1:p.Leu28504=
XM_017004821.1:c.85508T= (TTN) XP_016860310.1:p.Leu28503=
XM_017004822.1:c.82550T= (TTN) XP_016860311.1:p.Leu27517=
XM_017004823.1:c.64166T= (TTN) XP_016860312.1:p.Leu21389=
XM_024453094.1:c.85661T= (TTN) XP_024308862.1:p.Leu28554=
XM_024453095.1:c.85658T= (TTN) XP_024308863.1:p.Leu28553=
XM_024453096.1:c.85091T= (TTN) XP_024308864.1:p.Leu28364=
XM_024453097.1:c.82433T= (TTN) XP_024308865.1:p.Leu27478=
XM_024453098.1:c.82352T= (TTN) XP_024308866.1:p.Leu27451=
XM_024453099.1:c.64115T= (TTN) XP_024308867.1:p.Leu21372=
XM_024453100.1:c.53969T= (TTN) XP_024308868.1:p.Leu17990=