Canonical Allele Identifier: CA349405592

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98683G>T (TTN)	ENSP00000343764.6:p.Gly32895Ter
ENST00000342175.11:c.79768G>T (TTN)	ENSP00000340554.6:p.Gly26590Ter
ENST00000359218.10:c.79567G>T (TTN)	ENSP00000352154.5:p.Gly26523Ter
ENST00000342175.10:c.79768G>T (TTN)	ENSP00000340554.6:p.Gly26590Ter
ENST00000342992.10:c.98683G>T (TTN)	ENSP00000343764.6:p.Gly32895Ter
ENST00000359218.9:c.79567G>T (TTN)	ENSP00000352154.5:p.Gly26523Ter
ENST00000460472.6:c.79192G>T (TTN)	ENSP00000434586.1:p.Gly26398Ter
ENST00000589042.5:c.106387G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly35463Ter
ENST00000591111.5:c.101464G>T (TTN)	ENSP00000465570.1:p.Gly33822Ter
ENST00000615779.4:c.101464G>T (TTN)	ENSP00000483597.1:p.Gly33822Ter
NM_001256850.1:c.101464G>T (TTN)	NP_001243779.1:p.Gly33822Ter
NM_001267550.2:c.106387G>T (TTN) MANE Select	NP_001254479.2:p.Gly35463Ter
NM_003319.4:c.79192G>T (TTN)	NP_003310.4:p.Gly26398Ter
NM_133378.4:c.98683G>T (TTN)	NP_596869.4:p.Gly32895Ter
NM_133432.3:c.79567G>T (TTN)	NP_597676.3:p.Gly26523Ter
NM_133437.4:c.79768G>T (TTN)	NP_597681.4:p.Gly26590Ter
NR_038271.1:n.446+6468C>A (TTN-AS1)
NR_038272.1:n.220-5628C>A (TTN-AS1)
XM_011511729.1:c.105484G>T (TTN)	XP_011510031.1:p.Gly35162Ter
XM_011511730.1:c.79378G>T (TTN)	XP_011510032.1:p.Gly26460Ter
XM_011511731.1:c.79237G>T (TTN)	XP_011510033.1:p.Gly26413Ter
XM_017004819.1:c.105280G>T (TTN)	XP_016860308.1:p.Gly35094Ter
XM_017004820.1:c.100678G>T (TTN)	XP_016860309.1:p.Gly33560Ter
XM_017004821.1:c.100675G>T (TTN)	XP_016860310.1:p.Gly33559Ter
XM_017004822.1:c.97717G>T (TTN)	XP_016860311.1:p.Gly32573Ter
XM_017004823.1:c.79333G>T (TTN)	XP_016860312.1:p.Gly26445Ter
XM_024453094.1:c.100828G>T (TTN)	XP_024308862.1:p.Gly33610Ter
XM_024453095.1:c.100825G>T (TTN)	XP_024308863.1:p.Gly33609Ter
XM_024453096.1:c.100258G>T (TTN)	XP_024308864.1:p.Gly33420Ter
XM_024453097.1:c.97600G>T (TTN)	XP_024308865.1:p.Gly32534Ter
XM_024453098.1:c.97519G>T (TTN)	XP_024308866.1:p.Gly32507Ter
XM_024453099.1:c.79282G>T (TTN)	XP_024308867.1:p.Gly26428Ter
XM_024453100.1:c.69136G>T (TTN)	XP_024308868.1:p.Gly23046Ter