Canonical Allele Identifier: CA1310518088

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532120G= , CM000664.2:g.178532120G= GRCh38
NC_000002.11:g.179396847G= , CM000664.1:g.179396847G= GRCh37
NC_000002.10:g.179105093G= NCBI36
NG_011618.3:g.303683C= , LRG_391:g.303683C=
NG_051363.1:g.14294G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96791C= (TTN) ENSP00000343764.6:p.Ser32264=
ENST00000342175.11:c.77876C= (TTN) ENSP00000340554.6:p.Ser25959=
ENST00000359218.10:c.77675C= (TTN) ENSP00000352154.5:p.Ser25892=
ENST00000342175.10:c.77876C= (TTN) ENSP00000340554.6:p.Ser25959=
ENST00000342992.10:c.96791C= (TTN) ENSP00000343764.6:p.Ser32264=
ENST00000359218.9:c.77675C= (TTN) ENSP00000352154.5:p.Ser25892=
ENST00000460472.6:c.77300C= (TTN) ENSP00000434586.1:p.Ser25767=
ENST00000589042.5:c.104495C= (TTN) MANE Select ENSP00000467141.1:p.Ser34832=
ENST00000591111.5:c.99572C= (TTN) ENSP00000465570.1:p.Ser33191=
ENST00000615779.4:c.99572C= (TTN) ENSP00000483597.1:p.Ser33191=
NM_001256850.1:c.99572C= (TTN) NP_001243779.1:p.Ser33191=
NM_001267550.2:c.104495C= (TTN) MANE Select NP_001254479.2:p.Ser34832=
NM_003319.4:c.77300C= (TTN) NP_003310.4:p.Ser25767=
NM_133378.4:c.96791C= (TTN) NP_596869.4:p.Ser32264=
NM_133432.3:c.77675C= (TTN) NP_597676.3:p.Ser25892=
NM_133437.4:c.77876C= (TTN) NP_597681.4:p.Ser25959=
NR_038271.1:n.446+8484G= (TTN-AS1)
NR_038272.1:n.220-3612G= (TTN-AS1)
XM_011511729.1:c.103592C= (TTN) XP_011510031.1:p.Ser34531=
XM_011511730.1:c.77486C= (TTN) XP_011510032.1:p.Ser25829=
XM_011511731.1:c.77345C= (TTN) XP_011510033.1:p.Ser25782=
XM_017004819.1:c.103388C= (TTN) XP_016860308.1:p.Ser34463=
XM_017004820.1:c.98786C= (TTN) XP_016860309.1:p.Ser32929=
XM_017004821.1:c.98783C= (TTN) XP_016860310.1:p.Ser32928=
XM_017004822.1:c.95825C= (TTN) XP_016860311.1:p.Ser31942=
XM_017004823.1:c.77441C= (TTN) XP_016860312.1:p.Ser25814=
XM_024453094.1:c.98936C= (TTN) XP_024308862.1:p.Ser32979=
XM_024453095.1:c.98933C= (TTN) XP_024308863.1:p.Ser32978=
XM_024453096.1:c.98366C= (TTN) XP_024308864.1:p.Ser32789=
XM_024453097.1:c.95708C= (TTN) XP_024308865.1:p.Ser31903=
XM_024453098.1:c.95627C= (TTN) XP_024308866.1:p.Ser31876=
XM_024453099.1:c.77390C= (TTN) XP_024308867.1:p.Ser25797=
XM_024453100.1:c.67244C= (TTN) XP_024308868.1:p.Ser22415=