Canonical Allele Identifier: CA1310521177

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543910G= , CM000664.2:g.178543910G=	GRCh38
NC_000002.11:g.179408637G= , CM000664.1:g.179408637G=	GRCh37
NC_000002.10:g.179116883G=	NCBI36
NG_011618.3:g.291893C= , LRG_391:g.291893C=
NG_051363.1:g.26084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88530C= (TTN)	ENSP00000343764.6:p.Tyr29510=
ENST00000342175.11:c.69615C= (TTN)	ENSP00000340554.6:p.Tyr23205=
ENST00000359218.10:c.69414C= (TTN)	ENSP00000352154.5:p.Tyr23138=
ENST00000342175.10:c.69615C= (TTN)	ENSP00000340554.6:p.Tyr23205=
ENST00000342992.10:c.88530C= (TTN)	ENSP00000343764.6:p.Tyr29510=
ENST00000359218.9:c.69414C= (TTN)	ENSP00000352154.5:p.Tyr23138=
ENST00000460472.6:c.69039C= (TTN)	ENSP00000434586.1:p.Tyr23013=
ENST00000589042.5:c.96234C= (TTN) MANE Select	ENSP00000467141.1:p.Tyr32078=
ENST00000591111.5:c.91311C= (TTN)	ENSP00000465570.1:p.Tyr30437=
ENST00000615779.4:c.91311C= (TTN)	ENSP00000483597.1:p.Tyr30437=
NM_001256850.1:c.91311C= (TTN)	NP_001243779.1:p.Tyr30437=
NM_001267550.2:c.96234C= (TTN) MANE Select	NP_001254479.2:p.Tyr32078=
NM_003319.4:c.69039C= (TTN)	NP_003310.4:p.Tyr23013=
NM_133378.4:c.88530C= (TTN)	NP_596869.4:p.Tyr29510=
NM_133432.3:c.69414C= (TTN)	NP_597676.3:p.Tyr23138=
NM_133437.4:c.69615C= (TTN)	NP_597681.4:p.Tyr23205=
NR_038271.1:n.446+20274G= (TTN-AS1)
NR_038272.1:n.2043+1549G= (TTN-AS1)
XM_011511729.1:c.95331C= (TTN)	XP_011510031.1:p.Tyr31777=
XM_011511730.1:c.69225C= (TTN)	XP_011510032.1:p.Tyr23075=
XM_011511731.1:c.69084C= (TTN)	XP_011510033.1:p.Tyr23028=
XM_017004819.1:c.95127C= (TTN)	XP_016860308.1:p.Tyr31709=
XM_017004820.1:c.90525C= (TTN)	XP_016860309.1:p.Tyr30175=
XM_017004821.1:c.90522C= (TTN)	XP_016860310.1:p.Tyr30174=
XM_017004822.1:c.87564C= (TTN)	XP_016860311.1:p.Tyr29188=
XM_017004823.1:c.69180C= (TTN)	XP_016860312.1:p.Tyr23060=
XM_024453094.1:c.90675C= (TTN)	XP_024308862.1:p.Tyr30225=
XM_024453095.1:c.90672C= (TTN)	XP_024308863.1:p.Tyr30224=
XM_024453096.1:c.90105C= (TTN)	XP_024308864.1:p.Tyr30035=
XM_024453097.1:c.87447C= (TTN)	XP_024308865.1:p.Tyr29149=
XM_024453098.1:c.87366C= (TTN)	XP_024308866.1:p.Tyr29122=
XM_024453099.1:c.69129C= (TTN)	XP_024308867.1:p.Tyr23043=
XM_024453100.1:c.58983C= (TTN)	XP_024308868.1:p.Tyr19661=