Canonical Allele Identifier: CA1993496

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178601917A>G , CM000664.2:g.178601917A>G	GRCh38
NC_000002.11:g.179466644A>G , CM000664.1:g.179466644A>G	GRCh37
NC_000002.10:g.179174889A>G	NCBI36
NG_011618.3:g.233886T>C , LRG_391:g.233886T>C
NG_051363.1:g.84091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.47566-3T>C (TTN)	ENSP00000343764.6:n.47566-3T>C
ENST00000342175.11:c.28651-3T>C (TTN)	ENSP00000340554.6:n.28651-3T>C
ENST00000359218.10:c.28450-3T>C (TTN)	ENSP00000352154.5:n.28450-3T>C
ENST00000342175.10:c.28651-3T>C (TTN)	ENSP00000340554.6:n.28651-3T>C
ENST00000342992.10:c.47566-3T>C (TTN)	ENSP00000343764.6:n.47566-3T>C
ENST00000359218.9:c.28450-3T>C (TTN)	ENSP00000352154.5:n.28450-3T>C
ENST00000460472.6:c.28075-3T>C (TTN)	ENSP00000434586.1:n.28075-3T>C
ENST00000589042.5:c.55270-3T>C (TTN) MANE Select	ENSP00000467141.1:n.55270-3T>C
ENST00000591111.5:c.50347-3T>C (TTN)	ENSP00000465570.1:n.50347-3T>C
ENST00000615779.4:c.50347-3T>C (TTN)	ENSP00000483597.1:n.50347-3T>C
NM_001256850.1:c.50347-3T>C (TTN)	NP_001243779.1:n.50347-3T>C
NM_001267550.2:c.55270-3T>C (TTN) MANE Select	NP_001254479.2:n.55270-3T>C
NM_003319.4:c.28075-3T>C (TTN)	NP_003310.4:n.28075-3T>C
NM_133378.4:c.47566-3T>C (TTN)	NP_596869.4:n.47566-3T>C
NM_133432.3:c.28450-3T>C (TTN)	NP_597676.3:n.28450-3T>C
NM_133437.4:c.28651-3T>C (TTN)	NP_597681.4:n.28651-3T>C
NR_038271.1:n.682+4236A>G (TTN-AS1)
NR_038272.1:n.3917+1250A>G (TTN-AS1)
XM_011511729.1:c.54367-3T>C (TTN)	XP_011510031.1:n.54367-3T>C
XM_011511730.1:c.28261-3T>C (TTN)	XP_011510032.1:n.28261-3T>C
XM_011511731.1:c.28120-3T>C (TTN)	XP_011510033.1:n.28120-3T>C
XM_017004819.1:c.54163-3T>C (TTN)	XP_016860308.1:n.54163-3T>C
XM_017004820.1:c.49561-3T>C (TTN)	XP_016860309.1:n.49561-3T>C
XM_017004821.1:c.49558-3T>C (TTN)	XP_016860310.1:n.49558-3T>C
XM_017004822.1:c.46600-3T>C (TTN)	XP_016860311.1:n.46600-3T>C
XM_017004823.1:c.28216-3T>C (TTN)	XP_016860312.1:n.28216-3T>C
XM_024453094.1:c.49711-3T>C (TTN)	XP_024308862.1:n.49711-3T>C
XM_024453095.1:c.49708-3T>C (TTN)	XP_024308863.1:n.49708-3T>C
XM_024453096.1:c.49141-3T>C (TTN)	XP_024308864.1:n.49141-3T>C
XM_024453097.1:c.46483-3T>C (TTN)	XP_024308865.1:n.46483-3T>C
XM_024453098.1:c.46402-3T>C (TTN)	XP_024308866.1:n.46402-3T>C
XM_024453099.1:c.28165-3T>C (TTN)	XP_024308867.1:n.28165-3T>C
XM_024453100.1:c.18019-3T>C (TTN)	XP_024308868.1:n.18019-3T>C