Canonical Allele Identifier: CA349405590

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394831C>G (hg19) ; chr2:g.178530104C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530104C>G , CM000664.2:g.178530104C>G	GRCh38
NC_000002.11:g.179394831C>G , CM000664.1:g.179394831C>G	GRCh37
NC_000002.10:g.179103077C>G	NCBI36
NG_011618.3:g.305699G>C , LRG_391:g.305699G>C
NG_051363.1:g.12278C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98683G>C (TTN)	ENSP00000343764.6:p.Gly32895Arg
ENST00000342175.11:c.79768G>C (TTN)	ENSP00000340554.6:p.Gly26590Arg
ENST00000359218.10:c.79567G>C (TTN)	ENSP00000352154.5:p.Gly26523Arg
ENST00000342175.10:c.79768G>C (TTN)	ENSP00000340554.6:p.Gly26590Arg
ENST00000342992.10:c.98683G>C (TTN)	ENSP00000343764.6:p.Gly32895Arg
ENST00000359218.9:c.79567G>C (TTN)	ENSP00000352154.5:p.Gly26523Arg
ENST00000460472.6:c.79192G>C (TTN)	ENSP00000434586.1:p.Gly26398Arg
ENST00000589042.5:c.106387G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly35463Arg
ENST00000591111.5:c.101464G>C (TTN)	ENSP00000465570.1:p.Gly33822Arg
ENST00000615779.4:c.101464G>C (TTN)	ENSP00000483597.1:p.Gly33822Arg
NM_001256850.1:c.101464G>C (TTN)	NP_001243779.1:p.Gly33822Arg
NM_001267550.2:c.106387G>C (TTN) MANE Select	NP_001254479.2:p.Gly35463Arg
NM_003319.4:c.79192G>C (TTN)	NP_003310.4:p.Gly26398Arg
NM_133378.4:c.98683G>C (TTN)	NP_596869.4:p.Gly32895Arg
NM_133432.3:c.79567G>C (TTN)	NP_597676.3:p.Gly26523Arg
NM_133437.4:c.79768G>C (TTN)	NP_597681.4:p.Gly26590Arg
NR_038271.1:n.446+6468C>G (TTN-AS1)
NR_038272.1:n.220-5628C>G (TTN-AS1)
XM_011511729.1:c.105484G>C (TTN)	XP_011510031.1:p.Gly35162Arg
XM_011511730.1:c.79378G>C (TTN)	XP_011510032.1:p.Gly26460Arg
XM_011511731.1:c.79237G>C (TTN)	XP_011510033.1:p.Gly26413Arg
XM_017004819.1:c.105280G>C (TTN)	XP_016860308.1:p.Gly35094Arg
XM_017004820.1:c.100678G>C (TTN)	XP_016860309.1:p.Gly33560Arg
XM_017004821.1:c.100675G>C (TTN)	XP_016860310.1:p.Gly33559Arg
XM_017004822.1:c.97717G>C (TTN)	XP_016860311.1:p.Gly32573Arg
XM_017004823.1:c.79333G>C (TTN)	XP_016860312.1:p.Gly26445Arg
XM_024453094.1:c.100828G>C (TTN)	XP_024308862.1:p.Gly33610Arg
XM_024453095.1:c.100825G>C (TTN)	XP_024308863.1:p.Gly33609Arg
XM_024453096.1:c.100258G>C (TTN)	XP_024308864.1:p.Gly33420Arg
XM_024453097.1:c.97600G>C (TTN)	XP_024308865.1:p.Gly32534Arg
XM_024453098.1:c.97519G>C (TTN)	XP_024308866.1:p.Gly32507Arg
XM_024453099.1:c.79282G>C (TTN)	XP_024308867.1:p.Gly26428Arg
XM_024453100.1:c.69136G>C (TTN)	XP_024308868.1:p.Gly23046Arg