Canonical Allele Identifier: CA349618737

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482933T>G (hg19) ; chr2:g.178618206T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618206T>G , CM000664.2:g.178618206T>G	GRCh38
NC_000002.11:g.179482933T>G , CM000664.1:g.179482933T>G	GRCh37
NC_000002.10:g.179191178T>G	NCBI36
NG_011618.3:g.217597A>C , LRG_391:g.217597A>C
NG_051363.1:g.100380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39548A>C (TTN)	ENSP00000343764.6:p.Glu13183Ala
ENST00000342175.11:c.20633A>C (TTN)	ENSP00000340554.6:p.Glu6878Ala
ENST00000359218.10:c.20432A>C (TTN)	ENSP00000352154.5:p.Glu6811Ala
ENST00000342175.10:c.20633A>C (TTN)	ENSP00000340554.6:p.Glu6878Ala
ENST00000342992.10:c.39548A>C (TTN)	ENSP00000343764.6:p.Glu13183Ala
ENST00000359218.9:c.20432A>C (TTN)	ENSP00000352154.5:p.Glu6811Ala
ENST00000460472.6:c.20057A>C (TTN)	ENSP00000434586.1:p.Glu6686Ala
ENST00000589042.5:c.47252A>C (TTN) MANE Select	ENSP00000467141.1:p.Glu15751Ala
ENST00000591111.5:c.42329A>C (TTN)	ENSP00000465570.1:p.Glu14110Ala
ENST00000615779.4:c.42329A>C (TTN)	ENSP00000483597.1:p.Glu14110Ala
NM_001256850.1:c.42329A>C (TTN)	NP_001243779.1:p.Glu14110Ala
NM_001267550.2:c.47252A>C (TTN) MANE Select	NP_001254479.2:p.Glu15751Ala
NM_003319.4:c.20057A>C (TTN)	NP_003310.4:p.Glu6686Ala
NM_133378.4:c.39548A>C (TTN)	NP_596869.4:p.Glu13183Ala
NM_133432.3:c.20432A>C (TTN)	NP_597676.3:p.Glu6811Ala
NM_133437.4:c.20633A>C (TTN)	NP_597681.4:p.Glu6878Ala
NR_038271.1:n.1605-1547T>G (TTN-AS1)
XM_011511729.1:c.46349A>C (TTN)	XP_011510031.1:p.Glu15450Ala
XM_011511730.1:c.20243A>C (TTN)	XP_011510032.1:p.Glu6748Ala
XM_011511731.1:c.20102A>C (TTN)	XP_011510033.1:p.Glu6701Ala
XM_017004819.1:c.46145A>C (TTN)	XP_016860308.1:p.Glu15382Ala
XM_017004820.1:c.41543A>C (TTN)	XP_016860309.1:p.Glu13848Ala
XM_017004821.1:c.41540A>C (TTN)	XP_016860310.1:p.Glu13847Ala
XM_017004822.1:c.38582A>C (TTN)	XP_016860311.1:p.Glu12861Ala
XM_017004823.1:c.20198A>C (TTN)	XP_016860312.1:p.Glu6733Ala
XM_024453094.1:c.41693A>C (TTN)	XP_024308862.1:p.Glu13898Ala
XM_024453095.1:c.41690A>C (TTN)	XP_024308863.1:p.Glu13897Ala
XM_024453096.1:c.41123A>C (TTN)	XP_024308864.1:p.Glu13708Ala
XM_024453097.1:c.38465A>C (TTN)	XP_024308865.1:p.Glu12822Ala
XM_024453098.1:c.38384A>C (TTN)	XP_024308866.1:p.Glu12795Ala
XM_024453099.1:c.20147A>C (TTN)	XP_024308867.1:p.Glu6716Ala
XM_024453100.1:c.10001A>C (TTN)	XP_024308868.1:p.Glu3334Ala