Canonical Allele Identifier: CA430241490

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408592C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543865C>T , CM000664.2:g.178543865C>T	GRCh38
NC_000002.11:g.179408592C>T , CM000664.1:g.179408592C>T	GRCh37
NC_000002.10:g.179116838C>T	NCBI36
NG_011618.3:g.291938G>A , LRG_391:g.291938G>A
NG_051363.1:g.26039C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88575G>A (TTN)	ENSP00000343764.6:p.Lys29525=
ENST00000342175.11:c.69660G>A (TTN)	ENSP00000340554.6:p.Lys23220=
ENST00000359218.10:c.69459G>A (TTN)	ENSP00000352154.5:p.Lys23153=
ENST00000342175.10:c.69660G>A (TTN)	ENSP00000340554.6:p.Lys23220=
ENST00000342992.10:c.88575G>A (TTN)	ENSP00000343764.6:p.Lys29525=
ENST00000359218.9:c.69459G>A (TTN)	ENSP00000352154.5:p.Lys23153=
ENST00000460472.6:c.69084G>A (TTN)	ENSP00000434586.1:p.Lys23028=
ENST00000589042.5:c.96279G>A (TTN) MANE Select	ENSP00000467141.1:p.Lys32093=
ENST00000591111.5:c.91356G>A (TTN)	ENSP00000465570.1:p.Lys30452=
ENST00000615779.4:c.91356G>A (TTN)	ENSP00000483597.1:p.Lys30452=
NM_001256850.1:c.91356G>A (TTN)	NP_001243779.1:p.Lys30452=
NM_001267550.2:c.96279G>A (TTN) MANE Select	NP_001254479.2:p.Lys32093=
NM_003319.4:c.69084G>A (TTN)	NP_003310.4:p.Lys23028=
NM_133378.4:c.88575G>A (TTN)	NP_596869.4:p.Lys29525=
NM_133432.3:c.69459G>A (TTN)	NP_597676.3:p.Lys23153=
NM_133437.4:c.69660G>A (TTN)	NP_597681.4:p.Lys23220=
NR_038271.1:n.446+20229C>T (TTN-AS1)
NR_038272.1:n.2043+1504C>T (TTN-AS1)
XM_011511729.1:c.95376G>A (TTN)	XP_011510031.1:p.Lys31792=
XM_011511730.1:c.69270G>A (TTN)	XP_011510032.1:p.Lys23090=
XM_011511731.1:c.69129G>A (TTN)	XP_011510033.1:p.Lys23043=
XM_017004819.1:c.95172G>A (TTN)	XP_016860308.1:p.Lys31724=
XM_017004820.1:c.90570G>A (TTN)	XP_016860309.1:p.Lys30190=
XM_017004821.1:c.90567G>A (TTN)	XP_016860310.1:p.Lys30189=
XM_017004822.1:c.87609G>A (TTN)	XP_016860311.1:p.Lys29203=
XM_017004823.1:c.69225G>A (TTN)	XP_016860312.1:p.Lys23075=
XM_024453094.1:c.90720G>A (TTN)	XP_024308862.1:p.Lys30240=
XM_024453095.1:c.90717G>A (TTN)	XP_024308863.1:p.Lys30239=
XM_024453096.1:c.90150G>A (TTN)	XP_024308864.1:p.Lys30050=
XM_024453097.1:c.87492G>A (TTN)	XP_024308865.1:p.Lys29164=
XM_024453098.1:c.87411G>A (TTN)	XP_024308866.1:p.Lys29137=
XM_024453099.1:c.69174G>A (TTN)	XP_024308867.1:p.Lys23058=
XM_024453100.1:c.59028G>A (TTN)	XP_024308868.1:p.Lys19676=