Canonical Allele Identifier: CA349411732

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396904G>C (hg19) ; chr2:g.178532177G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532177G>C , CM000664.2:g.178532177G>C	GRCh38
NC_000002.11:g.179396904G>C , CM000664.1:g.179396904G>C	GRCh37
NC_000002.10:g.179105150G>C	NCBI36
NG_011618.3:g.303626C>G , LRG_391:g.303626C>G
NG_051363.1:g.14351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96734C>G (TTN)	ENSP00000343764.6:p.Thr32245Arg
ENST00000342175.11:c.77819C>G (TTN)	ENSP00000340554.6:p.Thr25940Arg
ENST00000359218.10:c.77618C>G (TTN)	ENSP00000352154.5:p.Thr25873Arg
ENST00000342175.10:c.77819C>G (TTN)	ENSP00000340554.6:p.Thr25940Arg
ENST00000342992.10:c.96734C>G (TTN)	ENSP00000343764.6:p.Thr32245Arg
ENST00000359218.9:c.77618C>G (TTN)	ENSP00000352154.5:p.Thr25873Arg
ENST00000460472.6:c.77243C>G (TTN)	ENSP00000434586.1:p.Thr25748Arg
ENST00000589042.5:c.104438C>G (TTN) MANE Select	ENSP00000467141.1:p.Thr34813Arg
ENST00000591111.5:c.99515C>G (TTN)	ENSP00000465570.1:p.Thr33172Arg
ENST00000615779.4:c.99515C>G (TTN)	ENSP00000483597.1:p.Thr33172Arg
NM_001256850.1:c.99515C>G (TTN)	NP_001243779.1:p.Thr33172Arg
NM_001267550.2:c.104438C>G (TTN) MANE Select	NP_001254479.2:p.Thr34813Arg
NM_003319.4:c.77243C>G (TTN)	NP_003310.4:p.Thr25748Arg
NM_133378.4:c.96734C>G (TTN)	NP_596869.4:p.Thr32245Arg
NM_133432.3:c.77618C>G (TTN)	NP_597676.3:p.Thr25873Arg
NM_133437.4:c.77819C>G (TTN)	NP_597681.4:p.Thr25940Arg
NR_038271.1:n.446+8541G>C (TTN-AS1)
NR_038272.1:n.220-3555G>C (TTN-AS1)
XM_011511729.1:c.103535C>G (TTN)	XP_011510031.1:p.Thr34512Arg
XM_011511730.1:c.77429C>G (TTN)	XP_011510032.1:p.Thr25810Arg
XM_011511731.1:c.77288C>G (TTN)	XP_011510033.1:p.Thr25763Arg
XM_017004819.1:c.103331C>G (TTN)	XP_016860308.1:p.Thr34444Arg
XM_017004820.1:c.98729C>G (TTN)	XP_016860309.1:p.Thr32910Arg
XM_017004821.1:c.98726C>G (TTN)	XP_016860310.1:p.Thr32909Arg
XM_017004822.1:c.95768C>G (TTN)	XP_016860311.1:p.Thr31923Arg
XM_017004823.1:c.77384C>G (TTN)	XP_016860312.1:p.Thr25795Arg
XM_024453094.1:c.98879C>G (TTN)	XP_024308862.1:p.Thr32960Arg
XM_024453095.1:c.98876C>G (TTN)	XP_024308863.1:p.Thr32959Arg
XM_024453096.1:c.98309C>G (TTN)	XP_024308864.1:p.Thr32770Arg
XM_024453097.1:c.95651C>G (TTN)	XP_024308865.1:p.Thr31884Arg
XM_024453098.1:c.95570C>G (TTN)	XP_024308866.1:p.Thr31857Arg
XM_024453099.1:c.77333C>G (TTN)	XP_024308867.1:p.Thr25778Arg
XM_024453100.1:c.67187C>G (TTN)	XP_024308868.1:p.Thr22396Arg