Canonical Allele Identifier: CA1310525932

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557804C= , CM000664.2:g.178557804C=	GRCh38
NC_000002.11:g.179422531C= , CM000664.1:g.179422531C=	GRCh37
NC_000002.10:g.179130777C=	NCBI36
NG_011618.3:g.277999G= , LRG_391:g.277999G=
NG_051363.1:g.39978C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.79846G= (TTN)	ENSP00000343764.6:p.Val26616=
ENST00000342175.11:c.60931G= (TTN)	ENSP00000340554.6:p.Val20311=
ENST00000359218.10:c.60730G= (TTN)	ENSP00000352154.5:p.Val20244=
ENST00000342175.10:c.60931G= (TTN)	ENSP00000340554.6:p.Val20311=
ENST00000342992.10:c.79846G= (TTN)	ENSP00000343764.6:p.Val26616=
ENST00000359218.9:c.60730G= (TTN)	ENSP00000352154.5:p.Val20244=
ENST00000460472.6:c.60355G= (TTN)	ENSP00000434586.1:p.Val20119=
ENST00000589042.5:c.87550G= (TTN) MANE Select	ENSP00000467141.1:p.Val29184=
ENST00000591111.5:c.82627G= (TTN)	ENSP00000465570.1:p.Val27543=
ENST00000615779.4:c.82627G= (TTN)	ENSP00000483597.1:p.Val27543=
NM_001256850.1:c.82627G= (TTN)	NP_001243779.1:p.Val27543=
NM_001267550.2:c.87550G= (TTN) MANE Select	NP_001254479.2:p.Val29184=
NM_003319.4:c.60355G= (TTN)	NP_003310.4:p.Val20119=
NM_133378.4:c.79846G= (TTN)	NP_596869.4:p.Val26616=
NM_133432.3:c.60730G= (TTN)	NP_597676.3:p.Val20244=
NM_133437.4:c.60931G= (TTN)	NP_597681.4:p.Val20311=
NR_038271.1:n.447-13496C= (TTN-AS1)
NR_038272.1:n.2043+15443C= (TTN-AS1)
XM_011511729.1:c.86647G= (TTN)	XP_011510031.1:p.Val28883=
XM_011511730.1:c.60541G= (TTN)	XP_011510032.1:p.Val20181=
XM_011511731.1:c.60400G= (TTN)	XP_011510033.1:p.Val20134=
XM_017004819.1:c.86443G= (TTN)	XP_016860308.1:p.Val28815=
XM_017004820.1:c.81841G= (TTN)	XP_016860309.1:p.Val27281=
XM_017004821.1:c.81838G= (TTN)	XP_016860310.1:p.Val27280=
XM_017004822.1:c.78880G= (TTN)	XP_016860311.1:p.Val26294=
XM_017004823.1:c.60496G= (TTN)	XP_016860312.1:p.Val20166=
XM_024453094.1:c.81991G= (TTN)	XP_024308862.1:p.Val27331=
XM_024453095.1:c.81988G= (TTN)	XP_024308863.1:p.Val27330=
XM_024453096.1:c.81421G= (TTN)	XP_024308864.1:p.Val27141=
XM_024453097.1:c.78763G= (TTN)	XP_024308865.1:p.Val26255=
XM_024453098.1:c.78682G= (TTN)	XP_024308866.1:p.Val26228=
XM_024453099.1:c.60445G= (TTN)	XP_024308867.1:p.Val20149=
XM_024453100.1:c.50299G= (TTN)	XP_024308868.1:p.Val16767=