Canonical Allele Identifier: CA349401547

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178528429T>C , CM000664.2:g.178528429T>C	GRCh38
NC_000002.11:g.179393156T>C , CM000664.1:g.179393156T>C	GRCh37
NC_000002.10:g.179101402T>C	NCBI36
NG_011618.3:g.307374A>G , LRG_391:g.307374A>G
NG_051363.1:g.10603T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107224-2A>G (TTN) MANE Select	NP_001254479.2:n.107224-2A>G
ENST00000589042.5:c.107224-2A>G (TTN) MANE Select	ENSP00000467141.1:n.107224-2A>G
NM_001256850.1:c.102301-2A>G (TTN)	NP_001243779.1:n.102301-2A>G
NM_003319.4:c.80029-2A>G (TTN)	NP_003310.4:n.80029-2A>G
NM_133378.4:c.99520-2A>G (TTN)	NP_596869.4:n.99520-2A>G
NM_133432.3:c.80404-2A>G (TTN)	NP_597676.3:n.80404-2A>G
NM_133437.4:c.80605-2A>G (TTN)	NP_597681.4:n.80605-2A>G
NR_038271.1:n.446+4793T>C (TTN-AS1)
NR_038272.1:n.219+4793T>C (TTN-AS1)
ENST00000342175.10:c.80605-2A>G (TTN)	ENSP00000340554.6:n.80605-2A>G
ENST00000342175.11:c.80605-2A>G (TTN)	ENSP00000340554.6:n.80605-2A>G
ENST00000342992.10:c.99520-2A>G (TTN)	ENSP00000343764.6:n.99520-2A>G
ENST00000342992.11:c.99520-2A>G (TTN)	ENSP00000343764.6:n.99520-2A>G
ENST00000359218.10:c.80404-2A>G (TTN)	ENSP00000352154.5:n.80404-2A>G
ENST00000359218.9:c.80404-2A>G (TTN)	ENSP00000352154.5:n.80404-2A>G
ENST00000460472.6:c.80029-2A>G (TTN)	ENSP00000434586.1:n.80029-2A>G
ENST00000591111.5:c.102301-2A>G (TTN)	ENSP00000465570.1:n.102301-2A>G
ENST00000615779.4:c.102301-2A>G (TTN)	ENSP00000483597.1:n.102301-2A>G
XM_011511729.1:c.106321-2A>G (TTN)	XP_011510031.1:n.106321-2A>G
XM_011511730.1:c.80215-2A>G (TTN)	XP_011510032.1:n.80215-2A>G
XM_011511731.1:c.80074-2A>G (TTN)	XP_011510033.1:n.80074-2A>G
XM_017004819.1:c.106117-2A>G (TTN)	XP_016860308.1:n.106117-2A>G
XM_017004820.1:c.101515-2A>G (TTN)	XP_016860309.1:n.101515-2A>G
XM_017004821.1:c.101512-2A>G (TTN)	XP_016860310.1:n.101512-2A>G
XM_017004822.1:c.98554-2A>G (TTN)	XP_016860311.1:n.98554-2A>G
XM_017004823.1:c.80170-2A>G (TTN)	XP_016860312.1:n.80170-2A>G
XM_024453094.1:c.101665-2A>G (TTN)	XP_024308862.1:n.101665-2A>G
XM_024453095.1:c.101662-2A>G (TTN)	XP_024308863.1:n.101662-2A>G
XM_024453096.1:c.101095-2A>G (TTN)	XP_024308864.1:n.101095-2A>G
XM_024453097.1:c.98437-2A>G (TTN)	XP_024308865.1:n.98437-2A>G
XM_024453098.1:c.98356-2A>G (TTN)	XP_024308866.1:n.98356-2A>G
XM_024453099.1:c.80119-2A>G (TTN)	XP_024308867.1:n.80119-2A>G
XM_024453100.1:c.69973-2A>G (TTN)	XP_024308868.1:n.69973-2A>G