Canonical Allele Identifier: CA349426053

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178580593T>A , CM000664.2:g.178580593T>A	GRCh38
NC_000002.11:g.179445320T>A , CM000664.1:g.179445320T>A	GRCh37
NC_000002.10:g.179153566T>A	NCBI36
NG_011618.3:g.255210A>T , LRG_391:g.255210A>T
NG_051363.1:g.62767T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66786A>T (TTN) MANE Select	NP_001254479.2:p.Glu22262Asp
ENST00000589042.5:c.66786A>T (TTN) MANE Select	ENSP00000467141.1:p.Glu22262Asp
NM_001256850.1:c.61863A>T (TTN)	NP_001243779.1:p.Glu20621Asp
NM_003319.4:c.39591A>T (TTN)	NP_003310.4:p.Glu13197Asp
NM_133378.4:c.59082A>T (TTN)	NP_596869.4:p.Glu19694Asp
NM_133432.3:c.39966A>T (TTN)	NP_597676.3:p.Glu13322Asp
NM_133437.4:c.40167A>T (TTN)	NP_597681.4:p.Glu13389Asp
NR_038271.1:n.596+9144T>A (TTN-AS1)
NR_038272.1:n.2044-1979T>A (TTN-AS1)
ENST00000342175.10:c.40167A>T (TTN)	ENSP00000340554.6:p.Glu13389Asp
ENST00000342175.11:c.40167A>T (TTN)	ENSP00000340554.6:p.Glu13389Asp
ENST00000342992.10:c.59082A>T (TTN)	ENSP00000343764.6:p.Glu19694Asp
ENST00000342992.11:c.59082A>T (TTN)	ENSP00000343764.6:p.Glu19694Asp
ENST00000359218.10:c.39966A>T (TTN)	ENSP00000352154.5:p.Glu13322Asp
ENST00000359218.9:c.39966A>T (TTN)	ENSP00000352154.5:p.Glu13322Asp
ENST00000460472.6:c.39591A>T (TTN)	ENSP00000434586.1:p.Glu13197Asp
ENST00000591111.5:c.61863A>T (TTN)	ENSP00000465570.1:p.Glu20621Asp
ENST00000615779.4:c.61863A>T (TTN)	ENSP00000483597.1:p.Glu20621Asp
XM_011511729.1:c.65883A>T (TTN)	XP_011510031.1:p.Glu21961Asp
XM_011511730.1:c.39777A>T (TTN)	XP_011510032.1:p.Glu13259Asp
XM_011511731.1:c.39636A>T (TTN)	XP_011510033.1:p.Glu13212Asp
XM_017004819.1:c.65679A>T (TTN)	XP_016860308.1:p.Glu21893Asp
XM_017004820.1:c.61077A>T (TTN)	XP_016860309.1:p.Glu20359Asp
XM_017004821.1:c.61074A>T (TTN)	XP_016860310.1:p.Glu20358Asp
XM_017004822.1:c.58116A>T (TTN)	XP_016860311.1:p.Glu19372Asp
XM_017004823.1:c.39732A>T (TTN)	XP_016860312.1:p.Glu13244Asp
XM_024453094.1:c.61227A>T (TTN)	XP_024308862.1:p.Glu20409Asp
XM_024453095.1:c.61224A>T (TTN)	XP_024308863.1:p.Glu20408Asp
XM_024453096.1:c.60657A>T (TTN)	XP_024308864.1:p.Glu20219Asp
XM_024453097.1:c.57999A>T (TTN)	XP_024308865.1:p.Glu19333Asp
XM_024453098.1:c.57918A>T (TTN)	XP_024308866.1:p.Glu19306Asp
XM_024453099.1:c.39681A>T (TTN)	XP_024308867.1:p.Glu13227Asp
XM_024453100.1:c.29535A>T (TTN)	XP_024308868.1:p.Glu9845Asp