Canonical Allele Identifier: CA349594586

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178566530C>T , CM000664.2:g.178566530C>T	GRCh38
NC_000002.11:g.179431257C>T , CM000664.1:g.179431257C>T	GRCh37
NC_000002.10:g.179139503C>T	NCBI36
NG_011618.3:g.269273G>A , LRG_391:g.269273G>A
NG_051363.1:g.48704C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.79602G>A (TTN) MANE Select	NP_001254479.2:p.Trp26534Ter
ENST00000589042.5:c.79602G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp26534Ter
NM_001256850.1:c.74679G>A (TTN)	NP_001243779.1:p.Trp24893Ter
NM_003319.4:c.52407G>A (TTN)	NP_003310.4:p.Trp17469Ter
NM_133378.4:c.71898G>A (TTN)	NP_596869.4:p.Trp23966Ter
NM_133432.3:c.52782G>A (TTN)	NP_597676.3:p.Trp17594Ter
NM_133437.4:c.52983G>A (TTN)	NP_597681.4:p.Trp17661Ter
NR_038271.1:n.447-4770C>T (TTN-AS1)
NR_038272.1:n.2044-16042C>T (TTN-AS1)
ENST00000342175.10:c.52983G>A (TTN)	ENSP00000340554.6:p.Trp17661Ter
ENST00000342175.11:c.52983G>A (TTN)	ENSP00000340554.6:p.Trp17661Ter
ENST00000342992.10:c.71898G>A (TTN)	ENSP00000343764.6:p.Trp23966Ter
ENST00000342992.11:c.71898G>A (TTN)	ENSP00000343764.6:p.Trp23966Ter
ENST00000359218.10:c.52782G>A (TTN)	ENSP00000352154.5:p.Trp17594Ter
ENST00000359218.9:c.52782G>A (TTN)	ENSP00000352154.5:p.Trp17594Ter
ENST00000460472.6:c.52407G>A (TTN)	ENSP00000434586.1:p.Trp17469Ter
ENST00000591111.5:c.74679G>A (TTN)	ENSP00000465570.1:p.Trp24893Ter
ENST00000615779.4:c.74679G>A (TTN)	ENSP00000483597.1:p.Trp24893Ter
XM_011511729.1:c.78699G>A (TTN)	XP_011510031.1:p.Trp26233Ter
XM_011511730.1:c.52593G>A (TTN)	XP_011510032.1:p.Trp17531Ter
XM_011511731.1:c.52452G>A (TTN)	XP_011510033.1:p.Trp17484Ter
XM_017004819.1:c.78495G>A (TTN)	XP_016860308.1:p.Trp26165Ter
XM_017004820.1:c.73893G>A (TTN)	XP_016860309.1:p.Trp24631Ter
XM_017004821.1:c.73890G>A (TTN)	XP_016860310.1:p.Trp24630Ter
XM_017004822.1:c.70932G>A (TTN)	XP_016860311.1:p.Trp23644Ter
XM_017004823.1:c.52548G>A (TTN)	XP_016860312.1:p.Trp17516Ter
XM_024453094.1:c.74043G>A (TTN)	XP_024308862.1:p.Trp24681Ter
XM_024453095.1:c.74040G>A (TTN)	XP_024308863.1:p.Trp24680Ter
XM_024453096.1:c.73473G>A (TTN)	XP_024308864.1:p.Trp24491Ter
XM_024453097.1:c.70815G>A (TTN)	XP_024308865.1:p.Trp23605Ter
XM_024453098.1:c.70734G>A (TTN)	XP_024308866.1:p.Trp23578Ter
XM_024453099.1:c.52497G>A (TTN)	XP_024308867.1:p.Trp17499Ter
XM_024453100.1:c.42351G>A (TTN)	XP_024308868.1:p.Trp14117Ter