Canonical Allele Identifier: CA430235195

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395277T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530550T>G , CM000664.2:g.178530550T>G	GRCh38
NC_000002.11:g.179395277T>G , CM000664.1:g.179395277T>G	GRCh37
NC_000002.10:g.179103523T>G	NCBI36
NG_011618.3:g.305253A>C , LRG_391:g.305253A>C
NG_051363.1:g.12724T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98361A>C (TTN)	ENSP00000343764.6:p.Gly32787=
ENST00000342175.11:c.79446A>C (TTN)	ENSP00000340554.6:p.Gly26482=
ENST00000359218.10:c.79245A>C (TTN)	ENSP00000352154.5:p.Gly26415=
ENST00000342175.10:c.79446A>C (TTN)	ENSP00000340554.6:p.Gly26482=
ENST00000342992.10:c.98361A>C (TTN)	ENSP00000343764.6:p.Gly32787=
ENST00000359218.9:c.79245A>C (TTN)	ENSP00000352154.5:p.Gly26415=
ENST00000460472.6:c.78870A>C (TTN)	ENSP00000434586.1:p.Gly26290=
ENST00000589042.5:c.106065A>C (TTN) MANE Select	ENSP00000467141.1:p.Gly35355=
ENST00000591111.5:c.101142A>C (TTN)	ENSP00000465570.1:p.Gly33714=
ENST00000615779.4:c.101142A>C (TTN)	ENSP00000483597.1:p.Gly33714=
NM_001256850.1:c.101142A>C (TTN)	NP_001243779.1:p.Gly33714=
NM_001267550.2:c.106065A>C (TTN) MANE Select	NP_001254479.2:p.Gly35355=
NM_003319.4:c.78870A>C (TTN)	NP_003310.4:p.Gly26290=
NM_133378.4:c.98361A>C (TTN)	NP_596869.4:p.Gly32787=
NM_133432.3:c.79245A>C (TTN)	NP_597676.3:p.Gly26415=
NM_133437.4:c.79446A>C (TTN)	NP_597681.4:p.Gly26482=
NR_038271.1:n.446+6914T>G (TTN-AS1)
NR_038272.1:n.220-5182T>G (TTN-AS1)
XM_011511729.1:c.105162A>C (TTN)	XP_011510031.1:p.Gly35054=
XM_011511730.1:c.79056A>C (TTN)	XP_011510032.1:p.Gly26352=
XM_011511731.1:c.78915A>C (TTN)	XP_011510033.1:p.Gly26305=
XM_017004819.1:c.104958A>C (TTN)	XP_016860308.1:p.Gly34986=
XM_017004820.1:c.100356A>C (TTN)	XP_016860309.1:p.Gly33452=
XM_017004821.1:c.100353A>C (TTN)	XP_016860310.1:p.Gly33451=
XM_017004822.1:c.97395A>C (TTN)	XP_016860311.1:p.Gly32465=
XM_017004823.1:c.79011A>C (TTN)	XP_016860312.1:p.Gly26337=
XM_024453094.1:c.100506A>C (TTN)	XP_024308862.1:p.Gly33502=
XM_024453095.1:c.100503A>C (TTN)	XP_024308863.1:p.Gly33501=
XM_024453096.1:c.99936A>C (TTN)	XP_024308864.1:p.Gly33312=
XM_024453097.1:c.97278A>C (TTN)	XP_024308865.1:p.Gly32426=
XM_024453098.1:c.97197A>C (TTN)	XP_024308866.1:p.Gly32399=
XM_024453099.1:c.78960A>C (TTN)	XP_024308867.1:p.Gly26320=
XM_024453100.1:c.68814A>C (TTN)	XP_024308868.1:p.Gly22938=