Canonical Allele Identifier: CA430244820

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1698598229
• MyVariant Identifiers: chr2:g.179414520G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549793G>A , CM000664.2:g.178549793G>A	GRCh38
NC_000002.11:g.179414520G>A , CM000664.1:g.179414520G>A	GRCh37
NC_000002.10:g.179122766G>A	NCBI36
NG_011618.3:g.286010C>T , LRG_391:g.286010C>T
NG_051363.1:g.31967G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84225C>T (TTN)	ENSP00000343764.6:p.Ala28075=
ENST00000342175.11:c.65310C>T (TTN)	ENSP00000340554.6:p.Ala21770=
ENST00000359218.10:c.65109C>T (TTN)	ENSP00000352154.5:p.Ala21703=
ENST00000342175.10:c.65310C>T (TTN)	ENSP00000340554.6:p.Ala21770=
ENST00000342992.10:c.84225C>T (TTN)	ENSP00000343764.6:p.Ala28075=
ENST00000359218.9:c.65109C>T (TTN)	ENSP00000352154.5:p.Ala21703=
ENST00000460472.6:c.64734C>T (TTN)	ENSP00000434586.1:p.Ala21578=
ENST00000589042.5:c.91929C>T (TTN) MANE Select	ENSP00000467141.1:p.Ala30643=
ENST00000591111.5:c.87006C>T (TTN)	ENSP00000465570.1:p.Ala29002=
ENST00000615779.4:c.87006C>T (TTN)	ENSP00000483597.1:p.Ala29002=
NM_001256850.1:c.87006C>T (TTN)	NP_001243779.1:p.Ala29002=
NM_001267550.2:c.91929C>T (TTN) MANE Select	NP_001254479.2:p.Ala30643=
NM_003319.4:c.64734C>T (TTN)	NP_003310.4:p.Ala21578=
NM_133378.4:c.84225C>T (TTN)	NP_596869.4:p.Ala28075=
NM_133432.3:c.65109C>T (TTN)	NP_597676.3:p.Ala21703=
NM_133437.4:c.65310C>T (TTN)	NP_597681.4:p.Ala21770=
NR_038271.1:n.447-21507G>A (TTN-AS1)
NR_038272.1:n.2043+7432G>A (TTN-AS1)
XM_011511729.1:c.91026C>T (TTN)	XP_011510031.1:p.Ala30342=
XM_011511730.1:c.64920C>T (TTN)	XP_011510032.1:p.Ala21640=
XM_011511731.1:c.64779C>T (TTN)	XP_011510033.1:p.Ala21593=
XM_017004819.1:c.90822C>T (TTN)	XP_016860308.1:p.Ala30274=
XM_017004820.1:c.86220C>T (TTN)	XP_016860309.1:p.Ala28740=
XM_017004821.1:c.86217C>T (TTN)	XP_016860310.1:p.Ala28739=
XM_017004822.1:c.83259C>T (TTN)	XP_016860311.1:p.Ala27753=
XM_017004823.1:c.64875C>T (TTN)	XP_016860312.1:p.Ala21625=
XM_024453094.1:c.86370C>T (TTN)	XP_024308862.1:p.Ala28790=
XM_024453095.1:c.86367C>T (TTN)	XP_024308863.1:p.Ala28789=
XM_024453096.1:c.85800C>T (TTN)	XP_024308864.1:p.Ala28600=
XM_024453097.1:c.83142C>T (TTN)	XP_024308865.1:p.Ala27714=
XM_024453098.1:c.83061C>T (TTN)	XP_024308866.1:p.Ala27687=
XM_024453099.1:c.64824C>T (TTN)	XP_024308867.1:p.Ala21608=
XM_024453100.1:c.54678C>T (TTN)	XP_024308868.1:p.Ala18226=