Canonical Allele Identifier: CA1310518157

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532272C= , CM000664.2:g.178532272C=	GRCh38
NC_000002.11:g.179396999C= , CM000664.1:g.179396999C=	GRCh37
NC_000002.10:g.179105245C=	NCBI36
NG_011618.3:g.303531G= , LRG_391:g.303531G=
NG_051363.1:g.14446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96639G= (TTN)	ENSP00000343764.6:p.Gln32213=
ENST00000342175.11:c.77724G= (TTN)	ENSP00000340554.6:p.Gln25908=
ENST00000359218.10:c.77523G= (TTN)	ENSP00000352154.5:p.Gln25841=
ENST00000342175.10:c.77724G= (TTN)	ENSP00000340554.6:p.Gln25908=
ENST00000342992.10:c.96639G= (TTN)	ENSP00000343764.6:p.Gln32213=
ENST00000359218.9:c.77523G= (TTN)	ENSP00000352154.5:p.Gln25841=
ENST00000460472.6:c.77148G= (TTN)	ENSP00000434586.1:p.Gln25716=
ENST00000589042.5:c.104343G= (TTN) MANE Select	ENSP00000467141.1:p.Gln34781=
ENST00000591111.5:c.99420G= (TTN)	ENSP00000465570.1:p.Gln33140=
ENST00000615779.4:c.99420G= (TTN)	ENSP00000483597.1:p.Gln33140=
NM_001256850.1:c.99420G= (TTN)	NP_001243779.1:p.Gln33140=
NM_001267550.2:c.104343G= (TTN) MANE Select	NP_001254479.2:p.Gln34781=
NM_003319.4:c.77148G= (TTN)	NP_003310.4:p.Gln25716=
NM_133378.4:c.96639G= (TTN)	NP_596869.4:p.Gln32213=
NM_133432.3:c.77523G= (TTN)	NP_597676.3:p.Gln25841=
NM_133437.4:c.77724G= (TTN)	NP_597681.4:p.Gln25908=
NR_038271.1:n.446+8636C= (TTN-AS1)
NR_038272.1:n.220-3460C= (TTN-AS1)
XM_011511729.1:c.103440G= (TTN)	XP_011510031.1:p.Gln34480=
XM_011511730.1:c.77334G= (TTN)	XP_011510032.1:p.Gln25778=
XM_011511731.1:c.77193G= (TTN)	XP_011510033.1:p.Gln25731=
XM_017004819.1:c.103236G= (TTN)	XP_016860308.1:p.Gln34412=
XM_017004820.1:c.98634G= (TTN)	XP_016860309.1:p.Gln32878=
XM_017004821.1:c.98631G= (TTN)	XP_016860310.1:p.Gln32877=
XM_017004822.1:c.95673G= (TTN)	XP_016860311.1:p.Gln31891=
XM_017004823.1:c.77289G= (TTN)	XP_016860312.1:p.Gln25763=
XM_024453094.1:c.98784G= (TTN)	XP_024308862.1:p.Gln32928=
XM_024453095.1:c.98781G= (TTN)	XP_024308863.1:p.Gln32927=
XM_024453096.1:c.98214G= (TTN)	XP_024308864.1:p.Gln32738=
XM_024453097.1:c.95556G= (TTN)	XP_024308865.1:p.Gln31852=
XM_024453098.1:c.95475G= (TTN)	XP_024308866.1:p.Gln31825=
XM_024453099.1:c.77238G= (TTN)	XP_024308867.1:p.Gln25746=
XM_024453100.1:c.67092G= (TTN)	XP_024308868.1:p.Gln22364=