Canonical Allele Identifier: CA430266669

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591488C>T , CM000664.2:g.178591488C>T	GRCh38
NC_000002.11:g.179456215C>T , CM000664.1:g.179456215C>T	GRCh37
NC_000002.10:g.179164461C>T	NCBI36
NG_011618.3:g.244315G>A , LRG_391:g.244315G>A
NG_051363.1:g.73662C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.60237G>A (TTN) MANE Select	NP_001254479.2:p.Glu20079=
ENST00000589042.5:c.60237G>A (TTN) MANE Select	ENSP00000467141.1:p.Glu20079=
NM_001256850.1:c.55314G>A (TTN)	NP_001243779.1:p.Glu18438=
NM_003319.4:c.33042G>A (TTN)	NP_003310.4:p.Glu11014=
NM_133378.4:c.52533G>A (TTN)	NP_596869.4:p.Glu17511=
NM_133432.3:c.33417G>A (TTN)	NP_597676.3:p.Glu11139=
NM_133437.4:c.33618G>A (TTN)	NP_597681.4:p.Glu11206=
NR_038271.1:n.597-6108C>T (TTN-AS1)
NR_038272.1:n.3364+174C>T (TTN-AS1)
ENST00000342175.10:c.33618G>A (TTN)	ENSP00000340554.6:p.Glu11206=
ENST00000342175.11:c.33618G>A (TTN)	ENSP00000340554.6:p.Glu11206=
ENST00000342992.10:c.52533G>A (TTN)	ENSP00000343764.6:p.Glu17511=
ENST00000342992.11:c.52533G>A (TTN)	ENSP00000343764.6:p.Glu17511=
ENST00000359218.10:c.33417G>A (TTN)	ENSP00000352154.5:p.Glu11139=
ENST00000359218.9:c.33417G>A (TTN)	ENSP00000352154.5:p.Glu11139=
ENST00000460472.6:c.33042G>A (TTN)	ENSP00000434586.1:p.Glu11014=
ENST00000591111.5:c.55314G>A (TTN)	ENSP00000465570.1:p.Glu18438=
ENST00000615779.4:c.55314G>A (TTN)	ENSP00000483597.1:p.Glu18438=
XM_011511729.1:c.59334G>A (TTN)	XP_011510031.1:p.Glu19778=
XM_011511730.1:c.33228G>A (TTN)	XP_011510032.1:p.Glu11076=
XM_011511731.1:c.33087G>A (TTN)	XP_011510033.1:p.Glu11029=
XM_017004819.1:c.59130G>A (TTN)	XP_016860308.1:p.Glu19710=
XM_017004820.1:c.54528G>A (TTN)	XP_016860309.1:p.Glu18176=
XM_017004821.1:c.54525G>A (TTN)	XP_016860310.1:p.Glu18175=
XM_017004822.1:c.51567G>A (TTN)	XP_016860311.1:p.Glu17189=
XM_017004823.1:c.33183G>A (TTN)	XP_016860312.1:p.Glu11061=
XM_024453094.1:c.54678G>A (TTN)	XP_024308862.1:p.Glu18226=
XM_024453095.1:c.54675G>A (TTN)	XP_024308863.1:p.Glu18225=
XM_024453096.1:c.54108G>A (TTN)	XP_024308864.1:p.Glu18036=
XM_024453097.1:c.51450G>A (TTN)	XP_024308865.1:p.Glu17150=
XM_024453098.1:c.51369G>A (TTN)	XP_024308866.1:p.Glu17123=
XM_024453099.1:c.33132G>A (TTN)	XP_024308867.1:p.Glu11044=
XM_024453100.1:c.22986G>A (TTN)	XP_024308868.1:p.Glu7662=