Canonical Allele Identifier: CA430244845

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179414547C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549820C>G , CM000664.2:g.178549820C>G	GRCh38
NC_000002.11:g.179414547C>G , CM000664.1:g.179414547C>G	GRCh37
NC_000002.10:g.179122793C>G	NCBI36
NG_011618.3:g.285983G>C , LRG_391:g.285983G>C
NG_051363.1:g.31994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84198G>C (TTN)	ENSP00000343764.6:p.Gly28066=
ENST00000342175.11:c.65283G>C (TTN)	ENSP00000340554.6:p.Gly21761=
ENST00000359218.10:c.65082G>C (TTN)	ENSP00000352154.5:p.Gly21694=
ENST00000342175.10:c.65283G>C (TTN)	ENSP00000340554.6:p.Gly21761=
ENST00000342992.10:c.84198G>C (TTN)	ENSP00000343764.6:p.Gly28066=
ENST00000359218.9:c.65082G>C (TTN)	ENSP00000352154.5:p.Gly21694=
ENST00000460472.6:c.64707G>C (TTN)	ENSP00000434586.1:p.Gly21569=
ENST00000589042.5:c.91902G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly30634=
ENST00000591111.5:c.86979G>C (TTN)	ENSP00000465570.1:p.Gly28993=
ENST00000615779.4:c.86979G>C (TTN)	ENSP00000483597.1:p.Gly28993=
NM_001256850.1:c.86979G>C (TTN)	NP_001243779.1:p.Gly28993=
NM_001267550.2:c.91902G>C (TTN) MANE Select	NP_001254479.2:p.Gly30634=
NM_003319.4:c.64707G>C (TTN)	NP_003310.4:p.Gly21569=
NM_133378.4:c.84198G>C (TTN)	NP_596869.4:p.Gly28066=
NM_133432.3:c.65082G>C (TTN)	NP_597676.3:p.Gly21694=
NM_133437.4:c.65283G>C (TTN)	NP_597681.4:p.Gly21761=
NR_038271.1:n.447-21480C>G (TTN-AS1)
NR_038272.1:n.2043+7459C>G (TTN-AS1)
XM_011511729.1:c.90999G>C (TTN)	XP_011510031.1:p.Gly30333=
XM_011511730.1:c.64893G>C (TTN)	XP_011510032.1:p.Gly21631=
XM_011511731.1:c.64752G>C (TTN)	XP_011510033.1:p.Gly21584=
XM_017004819.1:c.90795G>C (TTN)	XP_016860308.1:p.Gly30265=
XM_017004820.1:c.86193G>C (TTN)	XP_016860309.1:p.Gly28731=
XM_017004821.1:c.86190G>C (TTN)	XP_016860310.1:p.Gly28730=
XM_017004822.1:c.83232G>C (TTN)	XP_016860311.1:p.Gly27744=
XM_017004823.1:c.64848G>C (TTN)	XP_016860312.1:p.Gly21616=
XM_024453094.1:c.86343G>C (TTN)	XP_024308862.1:p.Gly28781=
XM_024453095.1:c.86340G>C (TTN)	XP_024308863.1:p.Gly28780=
XM_024453096.1:c.85773G>C (TTN)	XP_024308864.1:p.Gly28591=
XM_024453097.1:c.83115G>C (TTN)	XP_024308865.1:p.Gly27705=
XM_024453098.1:c.83034G>C (TTN)	XP_024308866.1:p.Gly27678=
XM_024453099.1:c.64797G>C (TTN)	XP_024308867.1:p.Gly21599=
XM_024453100.1:c.54651G>C (TTN)	XP_024308868.1:p.Gly18217=