Canonical Allele Identifier: CA1993494

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178601893C>T , CM000664.2:g.178601893C>T	GRCh38
NC_000002.11:g.179466620C>T , CM000664.1:g.179466620C>T	GRCh37
NC_000002.10:g.179174865C>T	NCBI36
NG_011618.3:g.233910G>A , LRG_391:g.233910G>A
NG_051363.1:g.84067C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.55291G>A (TTN) MANE Select	NP_001254479.2:p.Glu18431Lys
ENST00000589042.5:c.55291G>A (TTN) MANE Select	ENSP00000467141.1:p.Glu18431Lys
NM_001256850.1:c.50368G>A (TTN)	NP_001243779.1:p.Glu16790Lys
NM_003319.4:c.28096G>A (TTN)	NP_003310.4:p.Glu9366Lys
NM_133378.4:c.47587G>A (TTN)	NP_596869.4:p.Glu15863Lys
NM_133432.3:c.28471G>A (TTN)	NP_597676.3:p.Glu9491Lys
NM_133437.4:c.28672G>A (TTN)	NP_597681.4:p.Glu9558Lys
NR_038271.1:n.682+4212C>T (TTN-AS1)
NR_038272.1:n.3917+1226C>T (TTN-AS1)
ENST00000342175.10:c.28672G>A (TTN)	ENSP00000340554.6:p.Glu9558Lys
ENST00000342175.11:c.28672G>A (TTN)	ENSP00000340554.6:p.Glu9558Lys
ENST00000342992.10:c.47587G>A (TTN)	ENSP00000343764.6:p.Glu15863Lys
ENST00000342992.11:c.47587G>A (TTN)	ENSP00000343764.6:p.Glu15863Lys
ENST00000359218.10:c.28471G>A (TTN)	ENSP00000352154.5:p.Glu9491Lys
ENST00000359218.9:c.28471G>A (TTN)	ENSP00000352154.5:p.Glu9491Lys
ENST00000460472.6:c.28096G>A (TTN)	ENSP00000434586.1:p.Glu9366Lys
ENST00000591111.5:c.50368G>A (TTN)	ENSP00000465570.1:p.Glu16790Lys
ENST00000615779.4:c.50368G>A (TTN)	ENSP00000483597.1:p.Glu16790Lys
XM_011511729.1:c.54388G>A (TTN)	XP_011510031.1:p.Glu18130Lys
XM_011511730.1:c.28282G>A (TTN)	XP_011510032.1:p.Glu9428Lys
XM_011511731.1:c.28141G>A (TTN)	XP_011510033.1:p.Glu9381Lys
XM_017004819.1:c.54184G>A (TTN)	XP_016860308.1:p.Glu18062Lys
XM_017004820.1:c.49582G>A (TTN)	XP_016860309.1:p.Glu16528Lys
XM_017004821.1:c.49579G>A (TTN)	XP_016860310.1:p.Glu16527Lys
XM_017004822.1:c.46621G>A (TTN)	XP_016860311.1:p.Glu15541Lys
XM_017004823.1:c.28237G>A (TTN)	XP_016860312.1:p.Glu9413Lys
XM_024453094.1:c.49732G>A (TTN)	XP_024308862.1:p.Glu16578Lys
XM_024453095.1:c.49729G>A (TTN)	XP_024308863.1:p.Glu16577Lys
XM_024453096.1:c.49162G>A (TTN)	XP_024308864.1:p.Glu16388Lys
XM_024453097.1:c.46504G>A (TTN)	XP_024308865.1:p.Glu15502Lys
XM_024453098.1:c.46423G>A (TTN)	XP_024308866.1:p.Glu15475Lys
XM_024453099.1:c.28186G>A (TTN)	XP_024308867.1:p.Glu9396Lys
XM_024453100.1:c.18040G>A (TTN)	XP_024308868.1:p.Glu6014Lys