Canonical Allele Identifier: CA1310518138

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532234G= , CM000664.2:g.178532234G=	GRCh38
NC_000002.11:g.179396961G= , CM000664.1:g.179396961G=	GRCh37
NC_000002.10:g.179105207G=	NCBI36
NG_011618.3:g.303569C= , LRG_391:g.303569C=
NG_051363.1:g.14408G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96677C= (TTN)	ENSP00000343764.6:p.Ser32226=
ENST00000342175.11:c.77762C= (TTN)	ENSP00000340554.6:p.Ser25921=
ENST00000359218.10:c.77561C= (TTN)	ENSP00000352154.5:p.Ser25854=
ENST00000342175.10:c.77762C= (TTN)	ENSP00000340554.6:p.Ser25921=
ENST00000342992.10:c.96677C= (TTN)	ENSP00000343764.6:p.Ser32226=
ENST00000359218.9:c.77561C= (TTN)	ENSP00000352154.5:p.Ser25854=
ENST00000460472.6:c.77186C= (TTN)	ENSP00000434586.1:p.Ser25729=
ENST00000589042.5:c.104381C= (TTN) MANE Select	ENSP00000467141.1:p.Ser34794=
ENST00000591111.5:c.99458C= (TTN)	ENSP00000465570.1:p.Ser33153=
ENST00000615779.4:c.99458C= (TTN)	ENSP00000483597.1:p.Ser33153=
NM_001256850.1:c.99458C= (TTN)	NP_001243779.1:p.Ser33153=
NM_001267550.2:c.104381C= (TTN) MANE Select	NP_001254479.2:p.Ser34794=
NM_003319.4:c.77186C= (TTN)	NP_003310.4:p.Ser25729=
NM_133378.4:c.96677C= (TTN)	NP_596869.4:p.Ser32226=
NM_133432.3:c.77561C= (TTN)	NP_597676.3:p.Ser25854=
NM_133437.4:c.77762C= (TTN)	NP_597681.4:p.Ser25921=
NR_038271.1:n.446+8598G= (TTN-AS1)
NR_038272.1:n.220-3498G= (TTN-AS1)
XM_011511729.1:c.103478C= (TTN)	XP_011510031.1:p.Ser34493=
XM_011511730.1:c.77372C= (TTN)	XP_011510032.1:p.Ser25791=
XM_011511731.1:c.77231C= (TTN)	XP_011510033.1:p.Ser25744=
XM_017004819.1:c.103274C= (TTN)	XP_016860308.1:p.Ser34425=
XM_017004820.1:c.98672C= (TTN)	XP_016860309.1:p.Ser32891=
XM_017004821.1:c.98669C= (TTN)	XP_016860310.1:p.Ser32890=
XM_017004822.1:c.95711C= (TTN)	XP_016860311.1:p.Ser31904=
XM_017004823.1:c.77327C= (TTN)	XP_016860312.1:p.Ser25776=
XM_024453094.1:c.98822C= (TTN)	XP_024308862.1:p.Ser32941=
XM_024453095.1:c.98819C= (TTN)	XP_024308863.1:p.Ser32940=
XM_024453096.1:c.98252C= (TTN)	XP_024308864.1:p.Ser32751=
XM_024453097.1:c.95594C= (TTN)	XP_024308865.1:p.Ser31865=
XM_024453098.1:c.95513C= (TTN)	XP_024308866.1:p.Ser31838=
XM_024453099.1:c.77276C= (TTN)	XP_024308867.1:p.Ser25759=
XM_024453100.1:c.67130C= (TTN)	XP_024308868.1:p.Ser22377=