Canonical Allele Identifier: CA1310550807

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178617845G= , CM000664.2:g.178617845G=	GRCh38
NC_000002.11:g.179482572G= , CM000664.1:g.179482572G=	GRCh37
NC_000002.10:g.179190817G=	NCBI36
NG_011618.3:g.217958C= , LRG_391:g.217958C=
NG_051363.1:g.100019G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.47506C= (TTN) MANE Select	NP_001254479.2:p.Gln15836=
ENST00000589042.5:c.47506C= (TTN) MANE Select	ENSP00000467141.1:p.Gln15836=
NM_001256850.1:c.42583C= (TTN)	NP_001243779.1:p.Gln14195=
NM_003319.4:c.20311C= (TTN)	NP_003310.4:p.Gln6771=
NM_133378.4:c.39802C= (TTN)	NP_596869.4:p.Gln13268=
NM_133432.3:c.20686C= (TTN)	NP_597676.3:p.Gln6896=
NM_133437.4:c.20887C= (TTN)	NP_597681.4:p.Gln6963=
NR_038271.1:n.1605-1908G= (TTN-AS1)
ENST00000342175.10:c.20887C= (TTN)	ENSP00000340554.6:p.Gln6963=
ENST00000342175.11:c.20887C= (TTN)	ENSP00000340554.6:p.Gln6963=
ENST00000342992.10:c.39802C= (TTN)	ENSP00000343764.6:p.Gln13268=
ENST00000342992.11:c.39802C= (TTN)	ENSP00000343764.6:p.Gln13268=
ENST00000359218.10:c.20686C= (TTN)	ENSP00000352154.5:p.Gln6896=
ENST00000359218.9:c.20686C= (TTN)	ENSP00000352154.5:p.Gln6896=
ENST00000460472.6:c.20311C= (TTN)	ENSP00000434586.1:p.Gln6771=
ENST00000591111.5:c.42583C= (TTN)	ENSP00000465570.1:p.Gln14195=
ENST00000615779.4:c.42583C= (TTN)	ENSP00000483597.1:p.Gln14195=
XM_011511729.1:c.46603C= (TTN)	XP_011510031.1:p.Gln15535=
XM_011511730.1:c.20497C= (TTN)	XP_011510032.1:p.Gln6833=
XM_011511731.1:c.20356C= (TTN)	XP_011510033.1:p.Gln6786=
XM_017004819.1:c.46399C= (TTN)	XP_016860308.1:p.Gln15467=
XM_017004820.1:c.41797C= (TTN)	XP_016860309.1:p.Gln13933=
XM_017004821.1:c.41794C= (TTN)	XP_016860310.1:p.Gln13932=
XM_017004822.1:c.38836C= (TTN)	XP_016860311.1:p.Gln12946=
XM_017004823.1:c.20452C= (TTN)	XP_016860312.1:p.Gln6818=
XM_024453094.1:c.41947C= (TTN)	XP_024308862.1:p.Gln13983=
XM_024453095.1:c.41944C= (TTN)	XP_024308863.1:p.Gln13982=
XM_024453096.1:c.41377C= (TTN)	XP_024308864.1:p.Gln13793=
XM_024453097.1:c.38719C= (TTN)	XP_024308865.1:p.Gln12907=
XM_024453098.1:c.38638C= (TTN)	XP_024308866.1:p.Gln12880=
XM_024453099.1:c.20401C= (TTN)	XP_024308867.1:p.Gln6801=
XM_024453100.1:c.10255C= (TTN)	XP_024308868.1:p.Gln3419=