Canonical Allele Identifier: CA1310518099

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532143A= , CM000664.2:g.178532143A= GRCh38
NC_000002.11:g.179396870A= , CM000664.1:g.179396870A= GRCh37
NC_000002.10:g.179105116A= NCBI36
NG_011618.3:g.303660T= , LRG_391:g.303660T=
NG_051363.1:g.14317A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96768T= (TTN) ENSP00000343764.6:p.His32256=
ENST00000342175.11:c.77853T= (TTN) ENSP00000340554.6:p.His25951=
ENST00000359218.10:c.77652T= (TTN) ENSP00000352154.5:p.His25884=
ENST00000342175.10:c.77853T= (TTN) ENSP00000340554.6:p.His25951=
ENST00000342992.10:c.96768T= (TTN) ENSP00000343764.6:p.His32256=
ENST00000359218.9:c.77652T= (TTN) ENSP00000352154.5:p.His25884=
ENST00000460472.6:c.77277T= (TTN) ENSP00000434586.1:p.His25759=
ENST00000589042.5:c.104472T= (TTN) MANE Select ENSP00000467141.1:p.His34824=
ENST00000591111.5:c.99549T= (TTN) ENSP00000465570.1:p.His33183=
ENST00000615779.4:c.99549T= (TTN) ENSP00000483597.1:p.His33183=
NM_001256850.1:c.99549T= (TTN) NP_001243779.1:p.His33183=
NM_001267550.2:c.104472T= (TTN) MANE Select NP_001254479.2:p.His34824=
NM_003319.4:c.77277T= (TTN) NP_003310.4:p.His25759=
NM_133378.4:c.96768T= (TTN) NP_596869.4:p.His32256=
NM_133432.3:c.77652T= (TTN) NP_597676.3:p.His25884=
NM_133437.4:c.77853T= (TTN) NP_597681.4:p.His25951=
NR_038271.1:n.446+8507A= (TTN-AS1)
NR_038272.1:n.220-3589A= (TTN-AS1)
XM_011511729.1:c.103569T= (TTN) XP_011510031.1:p.His34523=
XM_011511730.1:c.77463T= (TTN) XP_011510032.1:p.His25821=
XM_011511731.1:c.77322T= (TTN) XP_011510033.1:p.His25774=
XM_017004819.1:c.103365T= (TTN) XP_016860308.1:p.His34455=
XM_017004820.1:c.98763T= (TTN) XP_016860309.1:p.His32921=
XM_017004821.1:c.98760T= (TTN) XP_016860310.1:p.His32920=
XM_017004822.1:c.95802T= (TTN) XP_016860311.1:p.His31934=
XM_017004823.1:c.77418T= (TTN) XP_016860312.1:p.His25806=
XM_024453094.1:c.98913T= (TTN) XP_024308862.1:p.His32971=
XM_024453095.1:c.98910T= (TTN) XP_024308863.1:p.His32970=
XM_024453096.1:c.98343T= (TTN) XP_024308864.1:p.His32781=
XM_024453097.1:c.95685T= (TTN) XP_024308865.1:p.His31895=
XM_024453098.1:c.95604T= (TTN) XP_024308866.1:p.His31868=
XM_024453099.1:c.77367T= (TTN) XP_024308867.1:p.His25789=
XM_024453100.1:c.67221T= (TTN) XP_024308868.1:p.His22407=