Canonical Allele Identifier: CA10606328

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178590732T>C , CM000664.2:g.178590732T>C	GRCh38
NC_000002.11:g.179455459T>C , CM000664.1:g.179455459T>C	GRCh37
NC_000002.10:g.179163705T>C	NCBI36
NG_011618.3:g.245071A>G , LRG_391:g.245071A>G
NG_051363.1:g.72906T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.60993A>G (TTN) MANE Select	NP_001254479.2:p.Arg20331=
ENST00000589042.5:c.60993A>G (TTN) MANE Select	ENSP00000467141.1:p.Arg20331=
NM_001256850.1:c.56070A>G (TTN)	NP_001243779.1:p.Arg18690=
NM_003319.4:c.33798A>G (TTN)	NP_003310.4:p.Arg11266=
NM_133378.4:c.53289A>G (TTN)	NP_596869.4:p.Arg17763=
NM_133432.3:c.34173A>G (TTN)	NP_597676.3:p.Arg11391=
NM_133437.4:c.34374A>G (TTN)	NP_597681.4:p.Arg11458=
NR_038271.1:n.597-6864T>C (TTN-AS1)
NR_038272.1:n.3189-407T>C (TTN-AS1)
ENST00000342175.10:c.34374A>G (TTN)	ENSP00000340554.6:p.Arg11458=
ENST00000342175.11:c.34374A>G (TTN)	ENSP00000340554.6:p.Arg11458=
ENST00000342992.10:c.53289A>G (TTN)	ENSP00000343764.6:p.Arg17763=
ENST00000342992.11:c.53289A>G (TTN)	ENSP00000343764.6:p.Arg17763=
ENST00000359218.10:c.34173A>G (TTN)	ENSP00000352154.5:p.Arg11391=
ENST00000359218.9:c.34173A>G (TTN)	ENSP00000352154.5:p.Arg11391=
ENST00000460472.6:c.33798A>G (TTN)	ENSP00000434586.1:p.Arg11266=
ENST00000591111.5:c.56070A>G (TTN)	ENSP00000465570.1:p.Arg18690=
ENST00000615779.4:c.56070A>G (TTN)	ENSP00000483597.1:p.Arg18690=
XM_011511729.1:c.60090A>G (TTN)	XP_011510031.1:p.Arg20030=
XM_011511730.1:c.33984A>G (TTN)	XP_011510032.1:p.Arg11328=
XM_011511731.1:c.33843A>G (TTN)	XP_011510033.1:p.Arg11281=
XM_017004819.1:c.59886A>G (TTN)	XP_016860308.1:p.Arg19962=
XM_017004820.1:c.55284A>G (TTN)	XP_016860309.1:p.Arg18428=
XM_017004821.1:c.55281A>G (TTN)	XP_016860310.1:p.Arg18427=
XM_017004822.1:c.52323A>G (TTN)	XP_016860311.1:p.Arg17441=
XM_017004823.1:c.33939A>G (TTN)	XP_016860312.1:p.Arg11313=
XM_024453094.1:c.55434A>G (TTN)	XP_024308862.1:p.Arg18478=
XM_024453095.1:c.55431A>G (TTN)	XP_024308863.1:p.Arg18477=
XM_024453096.1:c.54864A>G (TTN)	XP_024308864.1:p.Arg18288=
XM_024453097.1:c.52206A>G (TTN)	XP_024308865.1:p.Arg17402=
XM_024453098.1:c.52125A>G (TTN)	XP_024308866.1:p.Arg17375=
XM_024453099.1:c.33888A>G (TTN)	XP_024308867.1:p.Arg11296=
XM_024453100.1:c.23742A>G (TTN)	XP_024308868.1:p.Arg7914=