Canonical Allele Identifier: CA1310514656

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530472A= , CM000664.2:g.178530472A=	GRCh38
NC_000002.11:g.179395199A= , CM000664.1:g.179395199A=	GRCh37
NC_000002.10:g.179103445A=	NCBI36
NG_011618.3:g.305331T= , LRG_391:g.305331T=
NG_051363.1:g.12646A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98439T= (TTN)	ENSP00000343764.6:p.Ser32813=
ENST00000342175.11:c.79524T= (TTN)	ENSP00000340554.6:p.Ser26508=
ENST00000359218.10:c.79323T= (TTN)	ENSP00000352154.5:p.Ser26441=
ENST00000342175.10:c.79524T= (TTN)	ENSP00000340554.6:p.Ser26508=
ENST00000342992.10:c.98439T= (TTN)	ENSP00000343764.6:p.Ser32813=
ENST00000359218.9:c.79323T= (TTN)	ENSP00000352154.5:p.Ser26441=
ENST00000460472.6:c.78948T= (TTN)	ENSP00000434586.1:p.Ser26316=
ENST00000589042.5:c.106143T= (TTN) MANE Select	ENSP00000467141.1:p.Ser35381=
ENST00000591111.5:c.101220T= (TTN)	ENSP00000465570.1:p.Ser33740=
ENST00000615779.4:c.101220T= (TTN)	ENSP00000483597.1:p.Ser33740=
NM_001256850.1:c.101220T= (TTN)	NP_001243779.1:p.Ser33740=
NM_001267550.2:c.106143T= (TTN) MANE Select	NP_001254479.2:p.Ser35381=
NM_003319.4:c.78948T= (TTN)	NP_003310.4:p.Ser26316=
NM_133378.4:c.98439T= (TTN)	NP_596869.4:p.Ser32813=
NM_133432.3:c.79323T= (TTN)	NP_597676.3:p.Ser26441=
NM_133437.4:c.79524T= (TTN)	NP_597681.4:p.Ser26508=
NR_038271.1:n.446+6836A= (TTN-AS1)
NR_038272.1:n.220-5260A= (TTN-AS1)
XM_011511729.1:c.105240T= (TTN)	XP_011510031.1:p.Ser35080=
XM_011511730.1:c.79134T= (TTN)	XP_011510032.1:p.Ser26378=
XM_011511731.1:c.78993T= (TTN)	XP_011510033.1:p.Ser26331=
XM_017004819.1:c.105036T= (TTN)	XP_016860308.1:p.Ser35012=
XM_017004820.1:c.100434T= (TTN)	XP_016860309.1:p.Ser33478=
XM_017004821.1:c.100431T= (TTN)	XP_016860310.1:p.Ser33477=
XM_017004822.1:c.97473T= (TTN)	XP_016860311.1:p.Ser32491=
XM_017004823.1:c.79089T= (TTN)	XP_016860312.1:p.Ser26363=
XM_024453094.1:c.100584T= (TTN)	XP_024308862.1:p.Ser33528=
XM_024453095.1:c.100581T= (TTN)	XP_024308863.1:p.Ser33527=
XM_024453096.1:c.100014T= (TTN)	XP_024308864.1:p.Ser33338=
XM_024453097.1:c.97356T= (TTN)	XP_024308865.1:p.Ser32452=
XM_024453098.1:c.97275T= (TTN)	XP_024308866.1:p.Ser32425=
XM_024453099.1:c.79038T= (TTN)	XP_024308867.1:p.Ser26346=
XM_024453100.1:c.68892T= (TTN)	XP_024308868.1:p.Ser22964=