Canonical Allele Identifier: CA1310508271

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527598A= , CM000664.2:g.178527598A= GRCh38
NC_000002.11:g.179392325A= , CM000664.1:g.179392325A= GRCh37
NC_000002.10:g.179100571A= NCBI36
NG_011618.3:g.308205T= , LRG_391:g.308205T=
NG_051363.1:g.9772A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.99824T= (TTN) ENSP00000343764.6:p.Met33275=
ENST00000342175.11:c.80909T= (TTN) ENSP00000340554.6:p.Met26970=
ENST00000359218.10:c.80708T= (TTN) ENSP00000352154.5:p.Met26903=
ENST00000342175.10:c.80909T= (TTN) ENSP00000340554.6:p.Met26970=
ENST00000342992.10:c.99824T= (TTN) ENSP00000343764.6:p.Met33275=
ENST00000359218.9:c.80708T= (TTN) ENSP00000352154.5:p.Met26903=
ENST00000460472.6:c.80333T= (TTN) ENSP00000434586.1:p.Met26778=
ENST00000589042.5:c.107528T= (TTN) MANE Select ENSP00000467141.1:p.Met35843=
ENST00000591111.5:c.102605T= (TTN) ENSP00000465570.1:p.Met34202=
ENST00000615779.4:c.102605T= (TTN) ENSP00000483597.1:p.Met34202=
NM_001256850.1:c.102605T= (TTN) NP_001243779.1:p.Met34202=
NM_001267550.2:c.107528T= (TTN) MANE Select NP_001254479.2:p.Met35843=
NM_003319.4:c.80333T= (TTN) NP_003310.4:p.Met26778=
NM_133378.4:c.99824T= (TTN) NP_596869.4:p.Met33275=
NM_133432.3:c.80708T= (TTN) NP_597676.3:p.Met26903=
NM_133437.4:c.80909T= (TTN) NP_597681.4:p.Met26970=
NR_038271.1:n.446+3962A= (TTN-AS1)
NR_038272.1:n.219+3962A= (TTN-AS1)
XM_011511729.1:c.106625T= (TTN) XP_011510031.1:p.Met35542=
XM_011511730.1:c.80519T= (TTN) XP_011510032.1:p.Met26840=
XM_011511731.1:c.80378T= (TTN) XP_011510033.1:p.Met26793=
XM_017004819.1:c.106421T= (TTN) XP_016860308.1:p.Met35474=
XM_017004820.1:c.101819T= (TTN) XP_016860309.1:p.Met33940=
XM_017004821.1:c.101816T= (TTN) XP_016860310.1:p.Met33939=
XM_017004822.1:c.98858T= (TTN) XP_016860311.1:p.Met32953=
XM_017004823.1:c.80474T= (TTN) XP_016860312.1:p.Met26825=
XM_024453094.1:c.101969T= (TTN) XP_024308862.1:p.Met33990=
XM_024453095.1:c.101966T= (TTN) XP_024308863.1:p.Met33989=
XM_024453096.1:c.101399T= (TTN) XP_024308864.1:p.Met33800=
XM_024453097.1:c.98741T= (TTN) XP_024308865.1:p.Met32914=
XM_024453098.1:c.98660T= (TTN) XP_024308866.1:p.Met32887=
XM_024453099.1:c.80423T= (TTN) XP_024308867.1:p.Met26808=
XM_024453100.1:c.70277T= (TTN) XP_024308868.1:p.Met23426=