Canonical Allele Identifier: CA430254001

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179433723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568996T>C , CM000664.2:g.178568996T>C	GRCh38
NC_000002.11:g.179433723T>C , CM000664.1:g.179433723T>C	GRCh37
NC_000002.10:g.179141969T>C	NCBI36
NG_011618.3:g.266807A>G , LRG_391:g.266807A>G
NG_051363.1:g.51170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.69432A>G (TTN)	ENSP00000343764.6:p.Arg23144=
ENST00000342175.11:c.50517A>G (TTN)	ENSP00000340554.6:p.Arg16839=
ENST00000359218.10:c.50316A>G (TTN)	ENSP00000352154.5:p.Arg16772=
ENST00000342175.10:c.50517A>G (TTN)	ENSP00000340554.6:p.Arg16839=
ENST00000342992.10:c.69432A>G (TTN)	ENSP00000343764.6:p.Arg23144=
ENST00000359218.9:c.50316A>G (TTN)	ENSP00000352154.5:p.Arg16772=
ENST00000460472.6:c.49941A>G (TTN)	ENSP00000434586.1:p.Arg16647=
ENST00000589042.5:c.77136A>G (TTN) MANE Select	ENSP00000467141.1:p.Arg25712=
ENST00000591111.5:c.72213A>G (TTN)	ENSP00000465570.1:p.Arg24071=
ENST00000615779.4:c.72213A>G (TTN)	ENSP00000483597.1:p.Arg24071=
NM_001256850.1:c.72213A>G (TTN)	NP_001243779.1:p.Arg24071=
NM_001267550.2:c.77136A>G (TTN) MANE Select	NP_001254479.2:p.Arg25712=
NM_003319.4:c.49941A>G (TTN)	NP_003310.4:p.Arg16647=
NM_133378.4:c.69432A>G (TTN)	NP_596869.4:p.Arg23144=
NM_133432.3:c.50316A>G (TTN)	NP_597676.3:p.Arg16772=
NM_133437.4:c.50517A>G (TTN)	NP_597681.4:p.Arg16839=
NR_038271.1:n.447-2304T>C (TTN-AS1)
NR_038272.1:n.2044-13576T>C (TTN-AS1)
XM_011511729.1:c.76233A>G (TTN)	XP_011510031.1:p.Arg25411=
XM_011511730.1:c.50127A>G (TTN)	XP_011510032.1:p.Arg16709=
XM_011511731.1:c.49986A>G (TTN)	XP_011510033.1:p.Arg16662=
XM_017004819.1:c.76029A>G (TTN)	XP_016860308.1:p.Arg25343=
XM_017004820.1:c.71427A>G (TTN)	XP_016860309.1:p.Arg23809=
XM_017004821.1:c.71424A>G (TTN)	XP_016860310.1:p.Arg23808=
XM_017004822.1:c.68466A>G (TTN)	XP_016860311.1:p.Arg22822=
XM_017004823.1:c.50082A>G (TTN)	XP_016860312.1:p.Arg16694=
XM_024453094.1:c.71577A>G (TTN)	XP_024308862.1:p.Arg23859=
XM_024453095.1:c.71574A>G (TTN)	XP_024308863.1:p.Arg23858=
XM_024453096.1:c.71007A>G (TTN)	XP_024308864.1:p.Arg23669=
XM_024453097.1:c.68349A>G (TTN)	XP_024308865.1:p.Arg22783=
XM_024453098.1:c.68268A>G (TTN)	XP_024308866.1:p.Arg22756=
XM_024453099.1:c.50031A>G (TTN)	XP_024308867.1:p.Arg16677=
XM_024453100.1:c.39885A>G (TTN)	XP_024308868.1:p.Arg13295=