Canonical Allele Identifier: CA1991474

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178581688C>T , CM000664.2:g.178581688C>T	GRCh38
NC_000002.11:g.179446415C>T , CM000664.1:g.179446415C>T	GRCh37
NC_000002.10:g.179154661C>T	NCBI36
NG_011618.3:g.254115G>A , LRG_391:g.254115G>A
NG_051363.1:g.63862C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66580G>A (TTN) MANE Select	NP_001254479.2:p.Glu22194Lys
ENST00000589042.5:c.66580G>A (TTN) MANE Select	ENSP00000467141.1:p.Glu22194Lys
NM_001256850.1:c.61657G>A (TTN)	NP_001243779.1:p.Glu20553Lys
NM_003319.4:c.39385G>A (TTN)	NP_003310.4:p.Glu13129Lys
NM_133378.4:c.58876G>A (TTN)	NP_596869.4:p.Glu19626Lys
NM_133432.3:c.39760G>A (TTN)	NP_597676.3:p.Glu13254Lys
NM_133437.4:c.39961G>A (TTN)	NP_597681.4:p.Glu13321Lys
NR_038271.1:n.596+10239C>T (TTN-AS1)
NR_038272.1:n.2044-884C>T (TTN-AS1)
ENST00000342175.10:c.39961G>A (TTN)	ENSP00000340554.6:p.Glu13321Lys
ENST00000342175.11:c.39961G>A (TTN)	ENSP00000340554.6:p.Glu13321Lys
ENST00000342992.10:c.58876G>A (TTN)	ENSP00000343764.6:p.Glu19626Lys
ENST00000342992.11:c.58876G>A (TTN)	ENSP00000343764.6:p.Glu19626Lys
ENST00000359218.10:c.39760G>A (TTN)	ENSP00000352154.5:p.Glu13254Lys
ENST00000359218.9:c.39760G>A (TTN)	ENSP00000352154.5:p.Glu13254Lys
ENST00000460472.6:c.39385G>A (TTN)	ENSP00000434586.1:p.Glu13129Lys
ENST00000591111.5:c.61657G>A (TTN)	ENSP00000465570.1:p.Glu20553Lys
ENST00000615779.4:c.61657G>A (TTN)	ENSP00000483597.1:p.Glu20553Lys
XM_011511729.1:c.65677G>A (TTN)	XP_011510031.1:p.Glu21893Lys
XM_011511730.1:c.39571G>A (TTN)	XP_011510032.1:p.Glu13191Lys
XM_011511731.1:c.39430G>A (TTN)	XP_011510033.1:p.Glu13144Lys
XM_017004819.1:c.65473G>A (TTN)	XP_016860308.1:p.Glu21825Lys
XM_017004820.1:c.60871G>A (TTN)	XP_016860309.1:p.Glu20291Lys
XM_017004821.1:c.60868G>A (TTN)	XP_016860310.1:p.Glu20290Lys
XM_017004822.1:c.57910G>A (TTN)	XP_016860311.1:p.Glu19304Lys
XM_017004823.1:c.39526G>A (TTN)	XP_016860312.1:p.Glu13176Lys
XM_024453094.1:c.61021G>A (TTN)	XP_024308862.1:p.Glu20341Lys
XM_024453095.1:c.61018G>A (TTN)	XP_024308863.1:p.Glu20340Lys
XM_024453096.1:c.60451G>A (TTN)	XP_024308864.1:p.Glu20151Lys
XM_024453097.1:c.57793G>A (TTN)	XP_024308865.1:p.Glu19265Lys
XM_024453098.1:c.57712G>A (TTN)	XP_024308866.1:p.Glu19238Lys
XM_024453099.1:c.39475G>A (TTN)	XP_024308867.1:p.Glu13159Lys
XM_024453100.1:c.29329G>A (TTN)	XP_024308868.1:p.Glu9777Lys