Canonical Allele Identifier: CA1310518583

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178533241G= , CM000664.2:g.178533241G=	GRCh38
NC_000002.11:g.179397968G= , CM000664.1:g.179397968G=	GRCh37
NC_000002.10:g.179106214G=	NCBI36
NG_011618.3:g.302562C= , LRG_391:g.302562C=
NG_051363.1:g.15415G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.95670C= (TTN)	ENSP00000343764.6:p.Tyr31890=
ENST00000342175.11:c.76755C= (TTN)	ENSP00000340554.6:p.Tyr25585=
ENST00000359218.10:c.76554C= (TTN)	ENSP00000352154.5:p.Tyr25518=
ENST00000342175.10:c.76755C= (TTN)	ENSP00000340554.6:p.Tyr25585=
ENST00000342992.10:c.95670C= (TTN)	ENSP00000343764.6:p.Tyr31890=
ENST00000359218.9:c.76554C= (TTN)	ENSP00000352154.5:p.Tyr25518=
ENST00000460472.6:c.76179C= (TTN)	ENSP00000434586.1:p.Tyr25393=
ENST00000589042.5:c.103374C= (TTN) MANE Select	ENSP00000467141.1:p.Tyr34458=
ENST00000591111.5:c.98451C= (TTN)	ENSP00000465570.1:p.Tyr32817=
ENST00000615779.4:c.98451C= (TTN)	ENSP00000483597.1:p.Tyr32817=
NM_001256850.1:c.98451C= (TTN)	NP_001243779.1:p.Tyr32817=
NM_001267550.2:c.103374C= (TTN) MANE Select	NP_001254479.2:p.Tyr34458=
NM_003319.4:c.76179C= (TTN)	NP_003310.4:p.Tyr25393=
NM_133378.4:c.95670C= (TTN)	NP_596869.4:p.Tyr31890=
NM_133432.3:c.76554C= (TTN)	NP_597676.3:p.Tyr25518=
NM_133437.4:c.76755C= (TTN)	NP_597681.4:p.Tyr25585=
NR_038271.1:n.446+9605G= (TTN-AS1)
NR_038272.1:n.220-2491G= (TTN-AS1)
XM_011511729.1:c.102471C= (TTN)	XP_011510031.1:p.Tyr34157=
XM_011511730.1:c.76365C= (TTN)	XP_011510032.1:p.Tyr25455=
XM_011511731.1:c.76224C= (TTN)	XP_011510033.1:p.Tyr25408=
XM_017004819.1:c.102267C= (TTN)	XP_016860308.1:p.Tyr34089=
XM_017004820.1:c.97665C= (TTN)	XP_016860309.1:p.Tyr32555=
XM_017004821.1:c.97662C= (TTN)	XP_016860310.1:p.Tyr32554=
XM_017004822.1:c.94704C= (TTN)	XP_016860311.1:p.Tyr31568=
XM_017004823.1:c.76320C= (TTN)	XP_016860312.1:p.Tyr25440=
XM_024453094.1:c.97815C= (TTN)	XP_024308862.1:p.Tyr32605=
XM_024453095.1:c.97812C= (TTN)	XP_024308863.1:p.Tyr32604=
XM_024453096.1:c.97245C= (TTN)	XP_024308864.1:p.Tyr32415=
XM_024453097.1:c.94587C= (TTN)	XP_024308865.1:p.Tyr31529=
XM_024453098.1:c.94506C= (TTN)	XP_024308866.1:p.Tyr31502=
XM_024453099.1:c.76269C= (TTN)	XP_024308867.1:p.Tyr25423=
XM_024453100.1:c.66123C= (TTN)	XP_024308868.1:p.Tyr22041=