Canonical Allele Identifier: CA349515082

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178553016C>A , CM000664.2:g.178553016C>A	GRCh38
NC_000002.11:g.179417743C>A , CM000664.1:g.179417743C>A	GRCh37
NC_000002.10:g.179125989C>A	NCBI36
NG_011618.3:g.282787G>T , LRG_391:g.282787G>T
NG_051363.1:g.35190C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.89884G>T (TTN) MANE Select	NP_001254479.2:p.Gly29962Ter
ENST00000589042.5:c.89884G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly29962Ter
NM_001256850.1:c.84961G>T (TTN)	NP_001243779.1:p.Gly28321Ter
NM_003319.4:c.62689G>T (TTN)	NP_003310.4:p.Gly20897Ter
NM_133378.4:c.82180G>T (TTN)	NP_596869.4:p.Gly27394Ter
NM_133432.3:c.63064G>T (TTN)	NP_597676.3:p.Gly21022Ter
NM_133437.4:c.63265G>T (TTN)	NP_597681.4:p.Gly21089Ter
NR_038271.1:n.447-18284C>A (TTN-AS1)
NR_038272.1:n.2043+10655C>A (TTN-AS1)
ENST00000342175.10:c.63265G>T (TTN)	ENSP00000340554.6:p.Gly21089Ter
ENST00000342175.11:c.63265G>T (TTN)	ENSP00000340554.6:p.Gly21089Ter
ENST00000342992.10:c.82180G>T (TTN)	ENSP00000343764.6:p.Gly27394Ter
ENST00000342992.11:c.82180G>T (TTN)	ENSP00000343764.6:p.Gly27394Ter
ENST00000359218.10:c.63064G>T (TTN)	ENSP00000352154.5:p.Gly21022Ter
ENST00000359218.9:c.63064G>T (TTN)	ENSP00000352154.5:p.Gly21022Ter
ENST00000460472.6:c.62689G>T (TTN)	ENSP00000434586.1:p.Gly20897Ter
ENST00000591111.5:c.84961G>T (TTN)	ENSP00000465570.1:p.Gly28321Ter
ENST00000615779.4:c.84961G>T (TTN)	ENSP00000483597.1:p.Gly28321Ter
XM_011511729.1:c.88981G>T (TTN)	XP_011510031.1:p.Gly29661Ter
XM_011511730.1:c.62875G>T (TTN)	XP_011510032.1:p.Gly20959Ter
XM_011511731.1:c.62734G>T (TTN)	XP_011510033.1:p.Gly20912Ter
XM_017004819.1:c.88777G>T (TTN)	XP_016860308.1:p.Gly29593Ter
XM_017004820.1:c.84175G>T (TTN)	XP_016860309.1:p.Gly28059Ter
XM_017004821.1:c.84172G>T (TTN)	XP_016860310.1:p.Gly28058Ter
XM_017004822.1:c.81214G>T (TTN)	XP_016860311.1:p.Gly27072Ter
XM_017004823.1:c.62830G>T (TTN)	XP_016860312.1:p.Gly20944Ter
XM_024453094.1:c.84325G>T (TTN)	XP_024308862.1:p.Gly28109Ter
XM_024453095.1:c.84322G>T (TTN)	XP_024308863.1:p.Gly28108Ter
XM_024453096.1:c.83755G>T (TTN)	XP_024308864.1:p.Gly27919Ter
XM_024453097.1:c.81097G>T (TTN)	XP_024308865.1:p.Gly27033Ter
XM_024453098.1:c.81016G>T (TTN)	XP_024308866.1:p.Gly27006Ter
XM_024453099.1:c.62779G>T (TTN)	XP_024308867.1:p.Gly20927Ter
XM_024453100.1:c.52633G>T (TTN)	XP_024308868.1:p.Gly17545Ter