Canonical Allele Identifier: CA1310525937

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557812C= , CM000664.2:g.178557812C=	GRCh38
NC_000002.11:g.179422539C= , CM000664.1:g.179422539C=	GRCh37
NC_000002.10:g.179130785C=	NCBI36
NG_011618.3:g.277991G= , LRG_391:g.277991G=
NG_051363.1:g.39986C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.79838G= (TTN)	ENSP00000343764.6:p.Ser26613=
ENST00000342175.11:c.60923G= (TTN)	ENSP00000340554.6:p.Ser20308=
ENST00000359218.10:c.60722G= (TTN)	ENSP00000352154.5:p.Ser20241=
ENST00000342175.10:c.60923G= (TTN)	ENSP00000340554.6:p.Ser20308=
ENST00000342992.10:c.79838G= (TTN)	ENSP00000343764.6:p.Ser26613=
ENST00000359218.9:c.60722G= (TTN)	ENSP00000352154.5:p.Ser20241=
ENST00000460472.6:c.60347G= (TTN)	ENSP00000434586.1:p.Ser20116=
ENST00000589042.5:c.87542G= (TTN) MANE Select	ENSP00000467141.1:p.Ser29181=
ENST00000591111.5:c.82619G= (TTN)	ENSP00000465570.1:p.Ser27540=
ENST00000615779.4:c.82619G= (TTN)	ENSP00000483597.1:p.Ser27540=
NM_001256850.1:c.82619G= (TTN)	NP_001243779.1:p.Ser27540=
NM_001267550.2:c.87542G= (TTN) MANE Select	NP_001254479.2:p.Ser29181=
NM_003319.4:c.60347G= (TTN)	NP_003310.4:p.Ser20116=
NM_133378.4:c.79838G= (TTN)	NP_596869.4:p.Ser26613=
NM_133432.3:c.60722G= (TTN)	NP_597676.3:p.Ser20241=
NM_133437.4:c.60923G= (TTN)	NP_597681.4:p.Ser20308=
NR_038271.1:n.447-13488C= (TTN-AS1)
NR_038272.1:n.2043+15451C= (TTN-AS1)
XM_011511729.1:c.86639G= (TTN)	XP_011510031.1:p.Ser28880=
XM_011511730.1:c.60533G= (TTN)	XP_011510032.1:p.Ser20178=
XM_011511731.1:c.60392G= (TTN)	XP_011510033.1:p.Ser20131=
XM_017004819.1:c.86435G= (TTN)	XP_016860308.1:p.Ser28812=
XM_017004820.1:c.81833G= (TTN)	XP_016860309.1:p.Ser27278=
XM_017004821.1:c.81830G= (TTN)	XP_016860310.1:p.Ser27277=
XM_017004822.1:c.78872G= (TTN)	XP_016860311.1:p.Ser26291=
XM_017004823.1:c.60488G= (TTN)	XP_016860312.1:p.Ser20163=
XM_024453094.1:c.81983G= (TTN)	XP_024308862.1:p.Ser27328=
XM_024453095.1:c.81980G= (TTN)	XP_024308863.1:p.Ser27327=
XM_024453096.1:c.81413G= (TTN)	XP_024308864.1:p.Ser27138=
XM_024453097.1:c.78755G= (TTN)	XP_024308865.1:p.Ser26252=
XM_024453098.1:c.78674G= (TTN)	XP_024308866.1:p.Ser26225=
XM_024453099.1:c.60437G= (TTN)	XP_024308867.1:p.Ser20146=
XM_024453100.1:c.50291G= (TTN)	XP_024308868.1:p.Ser16764=