Canonical Allele Identifier: CA349545276

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179467069C>A (hg19) ; chr2:g.178602342C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178602342C>A , CM000664.2:g.178602342C>A	GRCh38
NC_000002.11:g.179467069C>A , CM000664.1:g.179467069C>A	GRCh37
NC_000002.10:g.179175314C>A	NCBI36
NG_011618.3:g.233461G>T , LRG_391:g.233461G>T
NG_051363.1:g.84516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.47356G>T (TTN)	ENSP00000343764.6:p.Glu15786Ter
ENST00000342175.11:c.28441G>T (TTN)	ENSP00000340554.6:p.Glu9481Ter
ENST00000359218.10:c.28240G>T (TTN)	ENSP00000352154.5:p.Glu9414Ter
ENST00000342175.10:c.28441G>T (TTN)	ENSP00000340554.6:p.Glu9481Ter
ENST00000342992.10:c.47356G>T (TTN)	ENSP00000343764.6:p.Glu15786Ter
ENST00000359218.9:c.28240G>T (TTN)	ENSP00000352154.5:p.Glu9414Ter
ENST00000460472.6:c.27865G>T (TTN)	ENSP00000434586.1:p.Glu9289Ter
ENST00000589042.5:c.55060G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu18354Ter
ENST00000591111.5:c.50137G>T (TTN)	ENSP00000465570.1:p.Glu16713Ter
ENST00000615779.4:c.50137G>T (TTN)	ENSP00000483597.1:p.Glu16713Ter
NM_001256850.1:c.50137G>T (TTN)	NP_001243779.1:p.Glu16713Ter
NM_001267550.2:c.55060G>T (TTN) MANE Select	NP_001254479.2:p.Glu18354Ter
NM_003319.4:c.27865G>T (TTN)	NP_003310.4:p.Glu9289Ter
NM_133378.4:c.47356G>T (TTN)	NP_596869.4:p.Glu15786Ter
NM_133432.3:c.28240G>T (TTN)	NP_597676.3:p.Glu9414Ter
NM_133437.4:c.28441G>T (TTN)	NP_597681.4:p.Glu9481Ter
NR_038271.1:n.682+4661C>A (TTN-AS1)
NR_038272.1:n.3917+1675C>A (TTN-AS1)
XM_011511729.1:c.54157G>T (TTN)	XP_011510031.1:p.Glu18053Ter
XM_011511730.1:c.28051G>T (TTN)	XP_011510032.1:p.Glu9351Ter
XM_011511731.1:c.27910G>T (TTN)	XP_011510033.1:p.Glu9304Ter
XM_017004819.1:c.53953G>T (TTN)	XP_016860308.1:p.Glu17985Ter
XM_017004820.1:c.49351G>T (TTN)	XP_016860309.1:p.Glu16451Ter
XM_017004821.1:c.49348G>T (TTN)	XP_016860310.1:p.Glu16450Ter
XM_017004822.1:c.46390G>T (TTN)	XP_016860311.1:p.Glu15464Ter
XM_017004823.1:c.28006G>T (TTN)	XP_016860312.1:p.Glu9336Ter
XM_024453094.1:c.49501G>T (TTN)	XP_024308862.1:p.Glu16501Ter
XM_024453095.1:c.49498G>T (TTN)	XP_024308863.1:p.Glu16500Ter
XM_024453096.1:c.48931G>T (TTN)	XP_024308864.1:p.Glu16311Ter
XM_024453097.1:c.46273G>T (TTN)	XP_024308865.1:p.Glu15425Ter
XM_024453098.1:c.46192G>T (TTN)	XP_024308866.1:p.Glu15398Ter
XM_024453099.1:c.27955G>T (TTN)	XP_024308867.1:p.Glu9319Ter
XM_024453100.1:c.17809G>T (TTN)	XP_024308868.1:p.Glu5937Ter