Canonical Allele Identifier: CA349628218

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179435675T>C (hg19) ; chr2:g.178570948T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570948T>C , CM000664.2:g.178570948T>C	GRCh38
NC_000002.11:g.179435675T>C , CM000664.1:g.179435675T>C	GRCh37
NC_000002.10:g.179143921T>C	NCBI36
NG_011618.3:g.264855A>G , LRG_391:g.264855A>G
NG_051363.1:g.53122T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.67480A>G (TTN)	ENSP00000343764.6:p.Ile22494Val
ENST00000342175.11:c.48565A>G (TTN)	ENSP00000340554.6:p.Ile16189Val
ENST00000359218.10:c.48364A>G (TTN)	ENSP00000352154.5:p.Ile16122Val
ENST00000342175.10:c.48565A>G (TTN)	ENSP00000340554.6:p.Ile16189Val
ENST00000342992.10:c.67480A>G (TTN)	ENSP00000343764.6:p.Ile22494Val
ENST00000359218.9:c.48364A>G (TTN)	ENSP00000352154.5:p.Ile16122Val
ENST00000460472.6:c.47989A>G (TTN)	ENSP00000434586.1:p.Ile15997Val
ENST00000589042.5:c.75184A>G (TTN) MANE Select	ENSP00000467141.1:p.Ile25062Val
ENST00000591111.5:c.70261A>G (TTN)	ENSP00000465570.1:p.Ile23421Val
ENST00000615779.4:c.70261A>G (TTN)	ENSP00000483597.1:p.Ile23421Val
NM_001256850.1:c.70261A>G (TTN)	NP_001243779.1:p.Ile23421Val
NM_001267550.2:c.75184A>G (TTN) MANE Select	NP_001254479.2:p.Ile25062Val
NM_003319.4:c.47989A>G (TTN)	NP_003310.4:p.Ile15997Val
NM_133378.4:c.67480A>G (TTN)	NP_596869.4:p.Ile22494Val
NM_133432.3:c.48364A>G (TTN)	NP_597676.3:p.Ile16122Val
NM_133437.4:c.48565A>G (TTN)	NP_597681.4:p.Ile16189Val
NR_038271.1:n.447-352T>C (TTN-AS1)
NR_038272.1:n.2044-11624T>C (TTN-AS1)
XM_011511729.1:c.74281A>G (TTN)	XP_011510031.1:p.Ile24761Val
XM_011511730.1:c.48175A>G (TTN)	XP_011510032.1:p.Ile16059Val
XM_011511731.1:c.48034A>G (TTN)	XP_011510033.1:p.Ile16012Val
XM_017004819.1:c.74077A>G (TTN)	XP_016860308.1:p.Ile24693Val
XM_017004820.1:c.69475A>G (TTN)	XP_016860309.1:p.Ile23159Val
XM_017004821.1:c.69472A>G (TTN)	XP_016860310.1:p.Ile23158Val
XM_017004822.1:c.66514A>G (TTN)	XP_016860311.1:p.Ile22172Val
XM_017004823.1:c.48130A>G (TTN)	XP_016860312.1:p.Ile16044Val
XM_024453094.1:c.69625A>G (TTN)	XP_024308862.1:p.Ile23209Val
XM_024453095.1:c.69622A>G (TTN)	XP_024308863.1:p.Ile23208Val
XM_024453096.1:c.69055A>G (TTN)	XP_024308864.1:p.Ile23019Val
XM_024453097.1:c.66397A>G (TTN)	XP_024308865.1:p.Ile22133Val
XM_024453098.1:c.66316A>G (TTN)	XP_024308866.1:p.Ile22106Val
XM_024453099.1:c.48079A>G (TTN)	XP_024308867.1:p.Ile16027Val
XM_024453100.1:c.37933A>G (TTN)	XP_024308868.1:p.Ile12645Val