Canonical Allele Identifier: CA309875

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178620048C>T , CM000664.2:g.178620048C>T	GRCh38
NC_000002.11:g.179484775C>T , CM000664.1:g.179484775C>T	GRCh37
NC_000002.10:g.179193020C>T	NCBI36
NG_011618.3:g.215755G>A , LRG_391:g.215755G>A
NG_051363.1:g.102222C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.46369G>A (TTN) MANE Select	NP_001254479.2:p.Glu15457Lys
ENST00000589042.5:c.46369G>A (TTN) MANE Select	ENSP00000467141.1:p.Glu15457Lys
NM_001256850.1:c.41446G>A (TTN)	NP_001243779.1:p.Glu13816Lys
NM_003319.4:c.19174G>A (TTN)	NP_003310.4:p.Glu6392Lys
NM_133378.4:c.38665G>A (TTN)	NP_596869.4:p.Glu12889Lys
NM_133432.3:c.19549G>A (TTN)	NP_597676.3:p.Glu6517Lys
NM_133437.4:c.19750G>A (TTN)	NP_597681.4:p.Glu6584Lys
NR_038271.1:n.1900C>T (TTN-AS1)
ENST00000342175.10:c.19750G>A (TTN)	ENSP00000340554.6:p.Glu6584Lys
ENST00000342175.11:c.19750G>A (TTN)	ENSP00000340554.6:p.Glu6584Lys
ENST00000342992.10:c.38665G>A (TTN)	ENSP00000343764.6:p.Glu12889Lys
ENST00000342992.11:c.38665G>A (TTN)	ENSP00000343764.6:p.Glu12889Lys
ENST00000359218.10:c.19549G>A (TTN)	ENSP00000352154.5:p.Glu6517Lys
ENST00000359218.9:c.19549G>A (TTN)	ENSP00000352154.5:p.Glu6517Lys
ENST00000460472.6:c.19174G>A (TTN)	ENSP00000434586.1:p.Glu6392Lys
ENST00000591111.5:c.41446G>A (TTN)	ENSP00000465570.1:p.Glu13816Lys
ENST00000615779.4:c.41446G>A (TTN)	ENSP00000483597.1:p.Glu13816Lys
XM_011511729.1:c.45466G>A (TTN)	XP_011510031.1:p.Glu15156Lys
XM_011511730.1:c.19360G>A (TTN)	XP_011510032.1:p.Glu6454Lys
XM_011511731.1:c.19219G>A (TTN)	XP_011510033.1:p.Glu6407Lys
XM_017004819.1:c.45262G>A (TTN)	XP_016860308.1:p.Glu15088Lys
XM_017004820.1:c.40660G>A (TTN)	XP_016860309.1:p.Glu13554Lys
XM_017004821.1:c.40657G>A (TTN)	XP_016860310.1:p.Glu13553Lys
XM_017004822.1:c.37699G>A (TTN)	XP_016860311.1:p.Glu12567Lys
XM_017004823.1:c.19315G>A (TTN)	XP_016860312.1:p.Glu6439Lys
XM_024453094.1:c.40810G>A (TTN)	XP_024308862.1:p.Glu13604Lys
XM_024453095.1:c.40807G>A (TTN)	XP_024308863.1:p.Glu13603Lys
XM_024453096.1:c.40240G>A (TTN)	XP_024308864.1:p.Glu13414Lys
XM_024453097.1:c.37582G>A (TTN)	XP_024308865.1:p.Glu12528Lys
XM_024453098.1:c.37501G>A (TTN)	XP_024308866.1:p.Glu12501Lys
XM_024453099.1:c.19264G>A (TTN)	XP_024308867.1:p.Glu6422Lys
XM_024453100.1:c.9118G>A (TTN)	XP_024308868.1:p.Glu3040Lys