Canonical Allele Identifier: CA349537119

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178558014T>A , CM000664.2:g.178558014T>A	GRCh38
NC_000002.11:g.179422741T>A , CM000664.1:g.179422741T>A	GRCh37
NC_000002.10:g.179130987T>A	NCBI36
NG_011618.3:g.277789A>T , LRG_391:g.277789A>T
NG_051363.1:g.40188T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.87340A>T (TTN) MANE Select	NP_001254479.2:p.Arg29114Ter
ENST00000589042.5:c.87340A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg29114Ter
NM_001256850.1:c.82417A>T (TTN)	NP_001243779.1:p.Arg27473Ter
NM_003319.4:c.60145A>T (TTN)	NP_003310.4:p.Arg20049Ter
NM_133378.4:c.79636A>T (TTN)	NP_596869.4:p.Arg26546Ter
NM_133432.3:c.60520A>T (TTN)	NP_597676.3:p.Arg20174Ter
NM_133437.4:c.60721A>T (TTN)	NP_597681.4:p.Arg20241Ter
NR_038271.1:n.447-13286T>A (TTN-AS1)
NR_038272.1:n.2043+15653T>A (TTN-AS1)
ENST00000342175.10:c.60721A>T (TTN)	ENSP00000340554.6:p.Arg20241Ter
ENST00000342175.11:c.60721A>T (TTN)	ENSP00000340554.6:p.Arg20241Ter
ENST00000342992.10:c.79636A>T (TTN)	ENSP00000343764.6:p.Arg26546Ter
ENST00000342992.11:c.79636A>T (TTN)	ENSP00000343764.6:p.Arg26546Ter
ENST00000359218.10:c.60520A>T (TTN)	ENSP00000352154.5:p.Arg20174Ter
ENST00000359218.9:c.60520A>T (TTN)	ENSP00000352154.5:p.Arg20174Ter
ENST00000460472.6:c.60145A>T (TTN)	ENSP00000434586.1:p.Arg20049Ter
ENST00000591111.5:c.82417A>T (TTN)	ENSP00000465570.1:p.Arg27473Ter
ENST00000615779.4:c.82417A>T (TTN)	ENSP00000483597.1:p.Arg27473Ter
XM_011511729.1:c.86437A>T (TTN)	XP_011510031.1:p.Arg28813Ter
XM_011511730.1:c.60331A>T (TTN)	XP_011510032.1:p.Arg20111Ter
XM_011511731.1:c.60190A>T (TTN)	XP_011510033.1:p.Arg20064Ter
XM_017004819.1:c.86233A>T (TTN)	XP_016860308.1:p.Arg28745Ter
XM_017004820.1:c.81631A>T (TTN)	XP_016860309.1:p.Arg27211Ter
XM_017004821.1:c.81628A>T (TTN)	XP_016860310.1:p.Arg27210Ter
XM_017004822.1:c.78670A>T (TTN)	XP_016860311.1:p.Arg26224Ter
XM_017004823.1:c.60286A>T (TTN)	XP_016860312.1:p.Arg20096Ter
XM_024453094.1:c.81781A>T (TTN)	XP_024308862.1:p.Arg27261Ter
XM_024453095.1:c.81778A>T (TTN)	XP_024308863.1:p.Arg27260Ter
XM_024453096.1:c.81211A>T (TTN)	XP_024308864.1:p.Arg27071Ter
XM_024453097.1:c.78553A>T (TTN)	XP_024308865.1:p.Arg26185Ter
XM_024453098.1:c.78472A>T (TTN)	XP_024308866.1:p.Arg26158Ter
XM_024453099.1:c.60235A>T (TTN)	XP_024308867.1:p.Arg20079Ter
XM_024453100.1:c.50089A>T (TTN)	XP_024308868.1:p.Arg16697Ter