Canonical Allele Identifier: CA349429470

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178582086G>C , CM000664.2:g.178582086G>C	GRCh38
NC_000002.11:g.179446813G>C , CM000664.1:g.179446813G>C	GRCh37
NC_000002.10:g.179155059G>C	NCBI36
NG_011618.3:g.253717C>G , LRG_391:g.253717C>G
NG_051363.1:g.64260G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66283C>G (TTN) MANE Select	NP_001254479.2:p.Arg22095Gly
ENST00000589042.5:c.66283C>G (TTN) MANE Select	ENSP00000467141.1:p.Arg22095Gly
NM_001256850.1:c.61360C>G (TTN)	NP_001243779.1:p.Arg20454Gly
NM_003319.4:c.39088C>G (TTN)	NP_003310.4:p.Arg13030Gly
NM_133378.4:c.58579C>G (TTN)	NP_596869.4:p.Arg19527Gly
NM_133432.3:c.39463C>G (TTN)	NP_597676.3:p.Arg13155Gly
NM_133437.4:c.39664C>G (TTN)	NP_597681.4:p.Arg13222Gly
NR_038271.1:n.596+10637G>C (TTN-AS1)
NR_038272.1:n.2044-486G>C (TTN-AS1)
ENST00000342175.10:c.39664C>G (TTN)	ENSP00000340554.6:p.Arg13222Gly
ENST00000342175.11:c.39664C>G (TTN)	ENSP00000340554.6:p.Arg13222Gly
ENST00000342992.10:c.58579C>G (TTN)	ENSP00000343764.6:p.Arg19527Gly
ENST00000342992.11:c.58579C>G (TTN)	ENSP00000343764.6:p.Arg19527Gly
ENST00000359218.10:c.39463C>G (TTN)	ENSP00000352154.5:p.Arg13155Gly
ENST00000359218.9:c.39463C>G (TTN)	ENSP00000352154.5:p.Arg13155Gly
ENST00000460472.6:c.39088C>G (TTN)	ENSP00000434586.1:p.Arg13030Gly
ENST00000591111.5:c.61360C>G (TTN)	ENSP00000465570.1:p.Arg20454Gly
ENST00000615779.4:c.61360C>G (TTN)	ENSP00000483597.1:p.Arg20454Gly
XM_011511729.1:c.65380C>G (TTN)	XP_011510031.1:p.Arg21794Gly
XM_011511730.1:c.39274C>G (TTN)	XP_011510032.1:p.Arg13092Gly
XM_011511731.1:c.39133C>G (TTN)	XP_011510033.1:p.Arg13045Gly
XM_017004819.1:c.65176C>G (TTN)	XP_016860308.1:p.Arg21726Gly
XM_017004820.1:c.60574C>G (TTN)	XP_016860309.1:p.Arg20192Gly
XM_017004821.1:c.60571C>G (TTN)	XP_016860310.1:p.Arg20191Gly
XM_017004822.1:c.57613C>G (TTN)	XP_016860311.1:p.Arg19205Gly
XM_017004823.1:c.39229C>G (TTN)	XP_016860312.1:p.Arg13077Gly
XM_024453094.1:c.60724C>G (TTN)	XP_024308862.1:p.Arg20242Gly
XM_024453095.1:c.60721C>G (TTN)	XP_024308863.1:p.Arg20241Gly
XM_024453096.1:c.60154C>G (TTN)	XP_024308864.1:p.Arg20052Gly
XM_024453097.1:c.57496C>G (TTN)	XP_024308865.1:p.Arg19166Gly
XM_024453098.1:c.57415C>G (TTN)	XP_024308866.1:p.Arg19139Gly
XM_024453099.1:c.39178C>G (TTN)	XP_024308867.1:p.Arg13060Gly
XM_024453100.1:c.29032C>G (TTN)	XP_024308868.1:p.Arg9678Gly