Canonical Allele Identifier: CA430235446

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395307T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530580T>C , CM000664.2:g.178530580T>C	GRCh38
NC_000002.11:g.179395307T>C , CM000664.1:g.179395307T>C	GRCh37
NC_000002.10:g.179103553T>C	NCBI36
NG_011618.3:g.305223A>G , LRG_391:g.305223A>G
NG_051363.1:g.12754T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98331A>G (TTN)	ENSP00000343764.6:p.Lys32777=
ENST00000342175.11:c.79416A>G (TTN)	ENSP00000340554.6:p.Lys26472=
ENST00000359218.10:c.79215A>G (TTN)	ENSP00000352154.5:p.Lys26405=
ENST00000342175.10:c.79416A>G (TTN)	ENSP00000340554.6:p.Lys26472=
ENST00000342992.10:c.98331A>G (TTN)	ENSP00000343764.6:p.Lys32777=
ENST00000359218.9:c.79215A>G (TTN)	ENSP00000352154.5:p.Lys26405=
ENST00000460472.6:c.78840A>G (TTN)	ENSP00000434586.1:p.Lys26280=
ENST00000589042.5:c.106035A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35345=
ENST00000591111.5:c.101112A>G (TTN)	ENSP00000465570.1:p.Lys33704=
ENST00000615779.4:c.101112A>G (TTN)	ENSP00000483597.1:p.Lys33704=
NM_001256850.1:c.101112A>G (TTN)	NP_001243779.1:p.Lys33704=
NM_001267550.2:c.106035A>G (TTN) MANE Select	NP_001254479.2:p.Lys35345=
NM_003319.4:c.78840A>G (TTN)	NP_003310.4:p.Lys26280=
NM_133378.4:c.98331A>G (TTN)	NP_596869.4:p.Lys32777=
NM_133432.3:c.79215A>G (TTN)	NP_597676.3:p.Lys26405=
NM_133437.4:c.79416A>G (TTN)	NP_597681.4:p.Lys26472=
NR_038271.1:n.446+6944T>C (TTN-AS1)
NR_038272.1:n.220-5152T>C (TTN-AS1)
XM_011511729.1:c.105132A>G (TTN)	XP_011510031.1:p.Lys35044=
XM_011511730.1:c.79026A>G (TTN)	XP_011510032.1:p.Lys26342=
XM_011511731.1:c.78885A>G (TTN)	XP_011510033.1:p.Lys26295=
XM_017004819.1:c.104928A>G (TTN)	XP_016860308.1:p.Lys34976=
XM_017004820.1:c.100326A>G (TTN)	XP_016860309.1:p.Lys33442=
XM_017004821.1:c.100323A>G (TTN)	XP_016860310.1:p.Lys33441=
XM_017004822.1:c.97365A>G (TTN)	XP_016860311.1:p.Lys32455=
XM_017004823.1:c.78981A>G (TTN)	XP_016860312.1:p.Lys26327=
XM_024453094.1:c.100476A>G (TTN)	XP_024308862.1:p.Lys33492=
XM_024453095.1:c.100473A>G (TTN)	XP_024308863.1:p.Lys33491=
XM_024453096.1:c.99906A>G (TTN)	XP_024308864.1:p.Lys33302=
XM_024453097.1:c.97248A>G (TTN)	XP_024308865.1:p.Lys32416=
XM_024453098.1:c.97167A>G (TTN)	XP_024308866.1:p.Lys32389=
XM_024453099.1:c.78930A>G (TTN)	XP_024308867.1:p.Lys26310=
XM_024453100.1:c.68784A>G (TTN)	XP_024308868.1:p.Lys22928=