Canonical Allele Identifier: CA1310549496

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614748G= , CM000664.2:g.178614748G=	GRCh38
NC_000002.11:g.179479475G= , CM000664.1:g.179479475G=	GRCh37
NC_000002.10:g.179187720G=	NCBI36
NG_011618.3:g.221055C= , LRG_391:g.221055C=
NG_051363.1:g.96922G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41062C= (TTN)	ENSP00000343764.6:p.Pro13688=
ENST00000342175.11:c.22147C= (TTN)	ENSP00000340554.6:p.Pro7383=
ENST00000359218.10:c.21946C= (TTN)	ENSP00000352154.5:p.Pro7316=
ENST00000342175.10:c.22147C= (TTN)	ENSP00000340554.6:p.Pro7383=
ENST00000342992.10:c.41062C= (TTN)	ENSP00000343764.6:p.Pro13688=
ENST00000359218.9:c.21946C= (TTN)	ENSP00000352154.5:p.Pro7316=
ENST00000460472.6:c.21571C= (TTN)	ENSP00000434586.1:p.Pro7191=
ENST00000589042.5:c.48766C= (TTN) MANE Select	ENSP00000467141.1:p.Pro16256=
ENST00000591111.5:c.43843C= (TTN)	ENSP00000465570.1:p.Pro14615=
ENST00000615779.4:c.43843C= (TTN)	ENSP00000483597.1:p.Pro14615=
NM_001256850.1:c.43843C= (TTN)	NP_001243779.1:p.Pro14615=
NM_001267550.2:c.48766C= (TTN) MANE Select	NP_001254479.2:p.Pro16256=
NM_003319.4:c.21571C= (TTN)	NP_003310.4:p.Pro7191=
NM_133378.4:c.41062C= (TTN)	NP_596869.4:p.Pro13688=
NM_133432.3:c.21946C= (TTN)	NP_597676.3:p.Pro7316=
NM_133437.4:c.22147C= (TTN)	NP_597681.4:p.Pro7383=
NR_038271.1:n.1496G= (TTN-AS1)
XM_011511729.1:c.47863C= (TTN)	XP_011510031.1:p.Pro15955=
XM_011511730.1:c.21757C= (TTN)	XP_011510032.1:p.Pro7253=
XM_011511731.1:c.21616C= (TTN)	XP_011510033.1:p.Pro7206=
XM_017004819.1:c.47659C= (TTN)	XP_016860308.1:p.Pro15887=
XM_017004820.1:c.43057C= (TTN)	XP_016860309.1:p.Pro14353=
XM_017004821.1:c.43054C= (TTN)	XP_016860310.1:p.Pro14352=
XM_017004822.1:c.40096C= (TTN)	XP_016860311.1:p.Pro13366=
XM_017004823.1:c.21712C= (TTN)	XP_016860312.1:p.Pro7238=
XM_024453094.1:c.43207C= (TTN)	XP_024308862.1:p.Pro14403=
XM_024453095.1:c.43204C= (TTN)	XP_024308863.1:p.Pro14402=
XM_024453096.1:c.42637C= (TTN)	XP_024308864.1:p.Pro14213=
XM_024453097.1:c.39979C= (TTN)	XP_024308865.1:p.Pro13327=
XM_024453098.1:c.39898C= (TTN)	XP_024308866.1:p.Pro13300=
XM_024453099.1:c.21661C= (TTN)	XP_024308867.1:p.Pro7221=
XM_024453100.1:c.11515C= (TTN)	XP_024308868.1:p.Pro3839=