Canonical Allele Identifier: CA1310520109

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549792G= , CM000664.2:g.178549792G=	GRCh38
NC_000002.11:g.179414519G= , CM000664.1:g.179414519G=	GRCh37
NC_000002.10:g.179122765G=	NCBI36
NG_011618.3:g.286011C= , LRG_391:g.286011C=
NG_051363.1:g.31966G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84226C= (TTN)	ENSP00000343764.6:p.Pro28076=
ENST00000342175.11:c.65311C= (TTN)	ENSP00000340554.6:p.Pro21771=
ENST00000359218.10:c.65110C= (TTN)	ENSP00000352154.5:p.Pro21704=
ENST00000342175.10:c.65311C= (TTN)	ENSP00000340554.6:p.Pro21771=
ENST00000342992.10:c.84226C= (TTN)	ENSP00000343764.6:p.Pro28076=
ENST00000359218.9:c.65110C= (TTN)	ENSP00000352154.5:p.Pro21704=
ENST00000460472.6:c.64735C= (TTN)	ENSP00000434586.1:p.Pro21579=
ENST00000589042.5:c.91930C= (TTN) MANE Select	ENSP00000467141.1:p.Pro30644=
ENST00000591111.5:c.87007C= (TTN)	ENSP00000465570.1:p.Pro29003=
ENST00000615779.4:c.87007C= (TTN)	ENSP00000483597.1:p.Pro29003=
NM_001256850.1:c.87007C= (TTN)	NP_001243779.1:p.Pro29003=
NM_001267550.2:c.91930C= (TTN) MANE Select	NP_001254479.2:p.Pro30644=
NM_003319.4:c.64735C= (TTN)	NP_003310.4:p.Pro21579=
NM_133378.4:c.84226C= (TTN)	NP_596869.4:p.Pro28076=
NM_133432.3:c.65110C= (TTN)	NP_597676.3:p.Pro21704=
NM_133437.4:c.65311C= (TTN)	NP_597681.4:p.Pro21771=
NR_038271.1:n.447-21508G= (TTN-AS1)
NR_038272.1:n.2043+7431G= (TTN-AS1)
XM_011511729.1:c.91027C= (TTN)	XP_011510031.1:p.Pro30343=
XM_011511730.1:c.64921C= (TTN)	XP_011510032.1:p.Pro21641=
XM_011511731.1:c.64780C= (TTN)	XP_011510033.1:p.Pro21594=
XM_017004819.1:c.90823C= (TTN)	XP_016860308.1:p.Pro30275=
XM_017004820.1:c.86221C= (TTN)	XP_016860309.1:p.Pro28741=
XM_017004821.1:c.86218C= (TTN)	XP_016860310.1:p.Pro28740=
XM_017004822.1:c.83260C= (TTN)	XP_016860311.1:p.Pro27754=
XM_017004823.1:c.64876C= (TTN)	XP_016860312.1:p.Pro21626=
XM_024453094.1:c.86371C= (TTN)	XP_024308862.1:p.Pro28791=
XM_024453095.1:c.86368C= (TTN)	XP_024308863.1:p.Pro28790=
XM_024453096.1:c.85801C= (TTN)	XP_024308864.1:p.Pro28601=
XM_024453097.1:c.83143C= (TTN)	XP_024308865.1:p.Pro27715=
XM_024453098.1:c.83062C= (TTN)	XP_024308866.1:p.Pro27688=
XM_024453099.1:c.64825C= (TTN)	XP_024308867.1:p.Pro21609=
XM_024453100.1:c.54679C= (TTN)	XP_024308868.1:p.Pro18227=