Canonical Allele Identifier: CA1310526074

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178558118G= , CM000664.2:g.178558118G=	GRCh38
NC_000002.11:g.179422845G= , CM000664.1:g.179422845G=	GRCh37
NC_000002.10:g.179131091G=	NCBI36
NG_011618.3:g.277685C= , LRG_391:g.277685C=
NG_051363.1:g.40292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.79532C= (TTN)	ENSP00000343764.6:p.Ser26511=
ENST00000342175.11:c.60617C= (TTN)	ENSP00000340554.6:p.Ser20206=
ENST00000359218.10:c.60416C= (TTN)	ENSP00000352154.5:p.Ser20139=
ENST00000342175.10:c.60617C= (TTN)	ENSP00000340554.6:p.Ser20206=
ENST00000342992.10:c.79532C= (TTN)	ENSP00000343764.6:p.Ser26511=
ENST00000359218.9:c.60416C= (TTN)	ENSP00000352154.5:p.Ser20139=
ENST00000460472.6:c.60041C= (TTN)	ENSP00000434586.1:p.Ser20014=
ENST00000589042.5:c.87236C= (TTN) MANE Select	ENSP00000467141.1:p.Ser29079=
ENST00000591111.5:c.82313C= (TTN)	ENSP00000465570.1:p.Ser27438=
ENST00000615779.4:c.82313C= (TTN)	ENSP00000483597.1:p.Ser27438=
NM_001256850.1:c.82313C= (TTN)	NP_001243779.1:p.Ser27438=
NM_001267550.2:c.87236C= (TTN) MANE Select	NP_001254479.2:p.Ser29079=
NM_003319.4:c.60041C= (TTN)	NP_003310.4:p.Ser20014=
NM_133378.4:c.79532C= (TTN)	NP_596869.4:p.Ser26511=
NM_133432.3:c.60416C= (TTN)	NP_597676.3:p.Ser20139=
NM_133437.4:c.60617C= (TTN)	NP_597681.4:p.Ser20206=
NR_038271.1:n.447-13182G= (TTN-AS1)
NR_038272.1:n.2043+15757G= (TTN-AS1)
XM_011511729.1:c.86333C= (TTN)	XP_011510031.1:p.Ser28778=
XM_011511730.1:c.60227C= (TTN)	XP_011510032.1:p.Ser20076=
XM_011511731.1:c.60086C= (TTN)	XP_011510033.1:p.Ser20029=
XM_017004819.1:c.86129C= (TTN)	XP_016860308.1:p.Ser28710=
XM_017004820.1:c.81527C= (TTN)	XP_016860309.1:p.Ser27176=
XM_017004821.1:c.81524C= (TTN)	XP_016860310.1:p.Ser27175=
XM_017004822.1:c.78566C= (TTN)	XP_016860311.1:p.Ser26189=
XM_017004823.1:c.60182C= (TTN)	XP_016860312.1:p.Ser20061=
XM_024453094.1:c.81677C= (TTN)	XP_024308862.1:p.Ser27226=
XM_024453095.1:c.81674C= (TTN)	XP_024308863.1:p.Ser27225=
XM_024453096.1:c.81107C= (TTN)	XP_024308864.1:p.Ser27036=
XM_024453097.1:c.78449C= (TTN)	XP_024308865.1:p.Ser26150=
XM_024453098.1:c.78368C= (TTN)	XP_024308866.1:p.Ser26123=
XM_024453099.1:c.60131C= (TTN)	XP_024308867.1:p.Ser20044=
XM_024453100.1:c.49985C= (TTN)	XP_024308868.1:p.Ser16662=