Canonical Allele Identifier: CA1310544484

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178602343A= , CM000664.2:g.178602343A= GRCh38
NC_000002.11:g.179467070A= , CM000664.1:g.179467070A= GRCh37
NC_000002.10:g.179175315A= NCBI36
NG_011618.3:g.233460T= , LRG_391:g.233460T=
NG_051363.1:g.84517A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.47355T= (TTN) ENSP00000343764.6:p.Asn15785=
ENST00000342175.11:c.28440T= (TTN) ENSP00000340554.6:p.Asn9480=
ENST00000359218.10:c.28239T= (TTN) ENSP00000352154.5:p.Asn9413=
ENST00000342175.10:c.28440T= (TTN) ENSP00000340554.6:p.Asn9480=
ENST00000342992.10:c.47355T= (TTN) ENSP00000343764.6:p.Asn15785=
ENST00000359218.9:c.28239T= (TTN) ENSP00000352154.5:p.Asn9413=
ENST00000460472.6:c.27864T= (TTN) ENSP00000434586.1:p.Asn9288=
ENST00000589042.5:c.55059T= (TTN) MANE Select ENSP00000467141.1:p.Asn18353=
ENST00000591111.5:c.50136T= (TTN) ENSP00000465570.1:p.Asn16712=
ENST00000615779.4:c.50136T= (TTN) ENSP00000483597.1:p.Asn16712=
NM_001256850.1:c.50136T= (TTN) NP_001243779.1:p.Asn16712=
NM_001267550.2:c.55059T= (TTN) MANE Select NP_001254479.2:p.Asn18353=
NM_003319.4:c.27864T= (TTN) NP_003310.4:p.Asn9288=
NM_133378.4:c.47355T= (TTN) NP_596869.4:p.Asn15785=
NM_133432.3:c.28239T= (TTN) NP_597676.3:p.Asn9413=
NM_133437.4:c.28440T= (TTN) NP_597681.4:p.Asn9480=
NR_038271.1:n.682+4662A= (TTN-AS1)
NR_038272.1:n.3917+1676A= (TTN-AS1)
XM_011511729.1:c.54156T= (TTN) XP_011510031.1:p.Asn18052=
XM_011511730.1:c.28050T= (TTN) XP_011510032.1:p.Asn9350=
XM_011511731.1:c.27909T= (TTN) XP_011510033.1:p.Asn9303=
XM_017004819.1:c.53952T= (TTN) XP_016860308.1:p.Asn17984=
XM_017004820.1:c.49350T= (TTN) XP_016860309.1:p.Asn16450=
XM_017004821.1:c.49347T= (TTN) XP_016860310.1:p.Asn16449=
XM_017004822.1:c.46389T= (TTN) XP_016860311.1:p.Asn15463=
XM_017004823.1:c.28005T= (TTN) XP_016860312.1:p.Asn9335=
XM_024453094.1:c.49500T= (TTN) XP_024308862.1:p.Asn16500=
XM_024453095.1:c.49497T= (TTN) XP_024308863.1:p.Asn16499=
XM_024453096.1:c.48930T= (TTN) XP_024308864.1:p.Asn16310=
XM_024453097.1:c.46272T= (TTN) XP_024308865.1:p.Asn15424=
XM_024453098.1:c.46191T= (TTN) XP_024308866.1:p.Asn15397=
XM_024453099.1:c.27954T= (TTN) XP_024308867.1:p.Asn9318=
XM_024453100.1:c.17808T= (TTN) XP_024308868.1:p.Asn5936=