Canonical Allele Identifier: CA349564645

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178562393G>T , CM000664.2:g.178562393G>T	GRCh38
NC_000002.11:g.179427120G>T , CM000664.1:g.179427120G>T	GRCh37
NC_000002.10:g.179135366G>T	NCBI36
NG_011618.3:g.273410C>A , LRG_391:g.273410C>A
NG_051363.1:g.44567G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.83739C>A (TTN) MANE Select	NP_001254479.2:p.Cys27913Ter
ENST00000589042.5:c.83739C>A (TTN) MANE Select	ENSP00000467141.1:p.Cys27913Ter
NM_001256850.1:c.78816C>A (TTN)	NP_001243779.1:p.Cys26272Ter
NM_003319.4:c.56544C>A (TTN)	NP_003310.4:p.Cys18848Ter
NM_133378.4:c.76035C>A (TTN)	NP_596869.4:p.Cys25345Ter
NM_133432.3:c.56919C>A (TTN)	NP_597676.3:p.Cys18973Ter
NM_133437.4:c.57120C>A (TTN)	NP_597681.4:p.Cys19040Ter
NR_038271.1:n.447-8907G>T (TTN-AS1)
NR_038272.1:n.2043+20032G>T (TTN-AS1)
ENST00000342175.10:c.57120C>A (TTN)	ENSP00000340554.6:p.Cys19040Ter
ENST00000342175.11:c.57120C>A (TTN)	ENSP00000340554.6:p.Cys19040Ter
ENST00000342992.10:c.76035C>A (TTN)	ENSP00000343764.6:p.Cys25345Ter
ENST00000342992.11:c.76035C>A (TTN)	ENSP00000343764.6:p.Cys25345Ter
ENST00000359218.10:c.56919C>A (TTN)	ENSP00000352154.5:p.Cys18973Ter
ENST00000359218.9:c.56919C>A (TTN)	ENSP00000352154.5:p.Cys18973Ter
ENST00000460472.6:c.56544C>A (TTN)	ENSP00000434586.1:p.Cys18848Ter
ENST00000591111.5:c.78816C>A (TTN)	ENSP00000465570.1:p.Cys26272Ter
ENST00000615779.4:c.78816C>A (TTN)	ENSP00000483597.1:p.Cys26272Ter
XM_011511729.1:c.82836C>A (TTN)	XP_011510031.1:p.Cys27612Ter
XM_011511730.1:c.56730C>A (TTN)	XP_011510032.1:p.Cys18910Ter
XM_011511731.1:c.56589C>A (TTN)	XP_011510033.1:p.Cys18863Ter
XM_017004819.1:c.82632C>A (TTN)	XP_016860308.1:p.Cys27544Ter
XM_017004820.1:c.78030C>A (TTN)	XP_016860309.1:p.Cys26010Ter
XM_017004821.1:c.78027C>A (TTN)	XP_016860310.1:p.Cys26009Ter
XM_017004822.1:c.75069C>A (TTN)	XP_016860311.1:p.Cys25023Ter
XM_017004823.1:c.56685C>A (TTN)	XP_016860312.1:p.Cys18895Ter
XM_024453094.1:c.78180C>A (TTN)	XP_024308862.1:p.Cys26060Ter
XM_024453095.1:c.78177C>A (TTN)	XP_024308863.1:p.Cys26059Ter
XM_024453096.1:c.77610C>A (TTN)	XP_024308864.1:p.Cys25870Ter
XM_024453097.1:c.74952C>A (TTN)	XP_024308865.1:p.Cys24984Ter
XM_024453098.1:c.74871C>A (TTN)	XP_024308866.1:p.Cys24957Ter
XM_024453099.1:c.56634C>A (TTN)	XP_024308867.1:p.Cys18878Ter
XM_024453100.1:c.46488C>A (TTN)	XP_024308868.1:p.Cys15496Ter