Canonical Allele Identifier: CA349524450

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179539812T>A (hg19) ; chr2:g.178675085T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178675085T>A , CM000664.2:g.178675085T>A	GRCh38
NC_000002.11:g.179539812T>A , CM000664.1:g.179539812T>A	GRCh37
NC_000002.10:g.179248057T>A	NCBI36
NG_011618.3:g.160718A>T , LRG_391:g.160718A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.30663A>T	ENSP00000343764.6:p.Glu10221Asp
ENST00000342175.11:c.13859-32768A>T	ENSP00000340554.6:n.13859-32768A>T
ENST00000359218.10:c.13658-32768A>T	ENSP00000352154.5:n.13658-32768A>T
ENST00000342175.10:c.13859-32768A>T	ENSP00000340554.6:n.13859-32768A>T
ENST00000342992.10:c.30663A>T	ENSP00000343764.6:p.Glu10221Asp
ENST00000359218.9:c.13658-32768A>T	ENSP00000352154.5:n.13658-32768A>T
ENST00000414766.5:c.2267-676A>T	ENSP00000401501.1:n.2267-676A>T
ENST00000460472.6:c.13283-32768A>T	ENSP00000434586.1:n.13283-32768A>T
ENST00000589042.5:c.34566A>T MANE Select	ENSP00000467141.1:p.Glu11522Asp
ENST00000591111.5:c.33444A>T	ENSP00000465570.1:p.Glu11148Asp
ENST00000615779.4:c.33444A>T	ENSP00000483597.1:p.Glu11148Asp
NM_001256850.1:c.33444A>T	NP_001243779.1:p.Glu11148Asp
NM_001267550.2:c.34566A>T MANE Select	NP_001254479.2:p.Glu11522Asp
NM_003319.4:c.13283-32768A>T	NP_003310.4:n.13283-32768A>T
NM_133378.4:c.30663A>T	NP_596869.4:p.Glu10221Asp
NM_133432.3:c.13658-32768A>T	NP_597676.3:n.13658-32768A>T
NM_133437.4:c.13859-32768A>T	NP_597681.4:n.13859-32768A>T
XM_011511729.1:c.33663A>T	XP_011510031.1:p.Glu11221Asp
XM_011511730.1:c.13469-32768A>T	XP_011510032.1:n.13469-32768A>T
XM_011511731.1:c.13328-32768A>T	XP_011510033.1:n.13328-32768A>T
XM_017004819.1:c.33618A>T	XP_016860308.1:p.Glu11206Asp
XM_017004820.1:c.30666A>T	XP_016860309.1:p.Glu10222Asp
XM_017004821.1:c.30663A>T	XP_016860310.1:p.Glu10221Asp
XM_017004822.1:c.31685-676A>T	XP_016860311.1:n.31685-676A>T
XM_017004823.1:c.13424-32768A>T	XP_016860312.1:n.13424-32768A>T
XM_024453094.1:c.33047-676A>T	XP_024308862.1:n.33047-676A>T
XM_024453095.1:c.33075A>T	XP_024308863.1:p.Glu11025Asp
XM_024453096.1:c.32477-676A>T	XP_024308864.1:n.32477-676A>T
XM_024453097.1:c.31517-676A>T	XP_024308865.1:n.31517-676A>T
XM_024453098.1:c.31436-676A>T	XP_024308866.1:n.31436-676A>T
XM_024453099.1:c.13424-32768A>T	XP_024308867.1:n.13424-32768A>T