Canonical Allele Identifier: CA430260260

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178579242T>C , CM000664.2:g.178579242T>C	GRCh38
NC_000002.11:g.179443969T>C , CM000664.1:g.179443969T>C	GRCh37
NC_000002.10:g.179152215T>C	NCBI36
NG_011618.3:g.256561A>G , LRG_391:g.256561A>G
NG_051363.1:g.61416T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.67788A>G (TTN) MANE Select	NP_001254479.2:p.Arg22596=
ENST00000589042.5:c.67788A>G (TTN) MANE Select	ENSP00000467141.1:p.Arg22596=
NM_001256850.1:c.62865A>G (TTN)	NP_001243779.1:p.Arg20955=
NM_003319.4:c.40593A>G (TTN)	NP_003310.4:p.Arg13531=
NM_133378.4:c.60084A>G (TTN)	NP_596869.4:p.Arg20028=
NM_133432.3:c.40968A>G (TTN)	NP_597676.3:p.Arg13656=
NM_133437.4:c.41169A>G (TTN)	NP_597681.4:p.Arg13723=
NR_038271.1:n.596+7793T>C (TTN-AS1)
NR_038272.1:n.2044-3330T>C (TTN-AS1)
ENST00000342175.10:c.41169A>G (TTN)	ENSP00000340554.6:p.Arg13723=
ENST00000342175.11:c.41169A>G (TTN)	ENSP00000340554.6:p.Arg13723=
ENST00000342992.10:c.60084A>G (TTN)	ENSP00000343764.6:p.Arg20028=
ENST00000342992.11:c.60084A>G (TTN)	ENSP00000343764.6:p.Arg20028=
ENST00000359218.10:c.40968A>G (TTN)	ENSP00000352154.5:p.Arg13656=
ENST00000359218.9:c.40968A>G (TTN)	ENSP00000352154.5:p.Arg13656=
ENST00000460472.6:c.40593A>G (TTN)	ENSP00000434586.1:p.Arg13531=
ENST00000591111.5:c.62865A>G (TTN)	ENSP00000465570.1:p.Arg20955=
ENST00000615779.4:c.62865A>G (TTN)	ENSP00000483597.1:p.Arg20955=
XM_011511729.1:c.66885A>G (TTN)	XP_011510031.1:p.Arg22295=
XM_011511730.1:c.40779A>G (TTN)	XP_011510032.1:p.Arg13593=
XM_011511731.1:c.40638A>G (TTN)	XP_011510033.1:p.Arg13546=
XM_017004819.1:c.66681A>G (TTN)	XP_016860308.1:p.Arg22227=
XM_017004820.1:c.62079A>G (TTN)	XP_016860309.1:p.Arg20693=
XM_017004821.1:c.62076A>G (TTN)	XP_016860310.1:p.Arg20692=
XM_017004822.1:c.59118A>G (TTN)	XP_016860311.1:p.Arg19706=
XM_017004823.1:c.40734A>G (TTN)	XP_016860312.1:p.Arg13578=
XM_024453094.1:c.62229A>G (TTN)	XP_024308862.1:p.Arg20743=
XM_024453095.1:c.62226A>G (TTN)	XP_024308863.1:p.Arg20742=
XM_024453096.1:c.61659A>G (TTN)	XP_024308864.1:p.Arg20553=
XM_024453097.1:c.59001A>G (TTN)	XP_024308865.1:p.Arg19667=
XM_024453098.1:c.58920A>G (TTN)	XP_024308866.1:p.Arg19640=
XM_024453099.1:c.40683A>G (TTN)	XP_024308867.1:p.Arg13561=
XM_024453100.1:c.30537A>G (TTN)	XP_024308868.1:p.Arg10179=