Canonical Allele Identifier: CA1310522536

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178553039C= , CM000664.2:g.178553039C=	GRCh38
NC_000002.11:g.179417766C= , CM000664.1:g.179417766C=	GRCh37
NC_000002.10:g.179126012C=	NCBI36
NG_011618.3:g.282764G= , LRG_391:g.282764G=
NG_051363.1:g.35213C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.82157G= (TTN)	ENSP00000343764.6:p.Trp27386=
ENST00000342175.11:c.63242G= (TTN)	ENSP00000340554.6:p.Trp21081=
ENST00000359218.10:c.63041G= (TTN)	ENSP00000352154.5:p.Trp21014=
ENST00000342175.10:c.63242G= (TTN)	ENSP00000340554.6:p.Trp21081=
ENST00000342992.10:c.82157G= (TTN)	ENSP00000343764.6:p.Trp27386=
ENST00000359218.9:c.63041G= (TTN)	ENSP00000352154.5:p.Trp21014=
ENST00000460472.6:c.62666G= (TTN)	ENSP00000434586.1:p.Trp20889=
ENST00000589042.5:c.89861G= (TTN) MANE Select	ENSP00000467141.1:p.Trp29954=
ENST00000591111.5:c.84938G= (TTN)	ENSP00000465570.1:p.Trp28313=
ENST00000615779.4:c.84938G= (TTN)	ENSP00000483597.1:p.Trp28313=
NM_001256850.1:c.84938G= (TTN)	NP_001243779.1:p.Trp28313=
NM_001267550.2:c.89861G= (TTN) MANE Select	NP_001254479.2:p.Trp29954=
NM_003319.4:c.62666G= (TTN)	NP_003310.4:p.Trp20889=
NM_133378.4:c.82157G= (TTN)	NP_596869.4:p.Trp27386=
NM_133432.3:c.63041G= (TTN)	NP_597676.3:p.Trp21014=
NM_133437.4:c.63242G= (TTN)	NP_597681.4:p.Trp21081=
NR_038271.1:n.447-18261C= (TTN-AS1)
NR_038272.1:n.2043+10678C= (TTN-AS1)
XM_011511729.1:c.88958G= (TTN)	XP_011510031.1:p.Trp29653=
XM_011511730.1:c.62852G= (TTN)	XP_011510032.1:p.Trp20951=
XM_011511731.1:c.62711G= (TTN)	XP_011510033.1:p.Trp20904=
XM_017004819.1:c.88754G= (TTN)	XP_016860308.1:p.Trp29585=
XM_017004820.1:c.84152G= (TTN)	XP_016860309.1:p.Trp28051=
XM_017004821.1:c.84149G= (TTN)	XP_016860310.1:p.Trp28050=
XM_017004822.1:c.81191G= (TTN)	XP_016860311.1:p.Trp27064=
XM_017004823.1:c.62807G= (TTN)	XP_016860312.1:p.Trp20936=
XM_024453094.1:c.84302G= (TTN)	XP_024308862.1:p.Trp28101=
XM_024453095.1:c.84299G= (TTN)	XP_024308863.1:p.Trp28100=
XM_024453096.1:c.83732G= (TTN)	XP_024308864.1:p.Trp27911=
XM_024453097.1:c.81074G= (TTN)	XP_024308865.1:p.Trp27025=
XM_024453098.1:c.80993G= (TTN)	XP_024308866.1:p.Trp26998=
XM_024453099.1:c.62756G= (TTN)	XP_024308867.1:p.Trp20919=
XM_024453100.1:c.52610G= (TTN)	XP_024308868.1:p.Trp17537=