Canonical Allele Identifier: CA1991062

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178577794C>T , CM000664.2:g.178577794C>T	GRCh38
NC_000002.11:g.179442521C>T , CM000664.1:g.179442521C>T	GRCh37
NC_000002.10:g.179150767C>T	NCBI36
NG_011618.3:g.258009G>A , LRG_391:g.258009G>A
NG_051363.1:g.59968C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.68632G>A (TTN) MANE Select	NP_001254479.2:p.Val22878Met
ENST00000589042.5:c.68632G>A (TTN) MANE Select	ENSP00000467141.1:p.Val22878Met
NM_001256850.1:c.63709G>A (TTN)	NP_001243779.1:p.Val21237Met
NM_003319.4:c.41437G>A (TTN)	NP_003310.4:p.Val13813Met
NM_133378.4:c.60928G>A (TTN)	NP_596869.4:p.Val20310Met
NM_133432.3:c.41812G>A (TTN)	NP_597676.3:p.Val13938Met
NM_133437.4:c.42013G>A (TTN)	NP_597681.4:p.Val14005Met
NR_038271.1:n.596+6345C>T (TTN-AS1)
NR_038272.1:n.2044-4778C>T (TTN-AS1)
ENST00000342175.10:c.42013G>A (TTN)	ENSP00000340554.6:p.Val14005Met
ENST00000342175.11:c.42013G>A (TTN)	ENSP00000340554.6:p.Val14005Met
ENST00000342992.10:c.60928G>A (TTN)	ENSP00000343764.6:p.Val20310Met
ENST00000342992.11:c.60928G>A (TTN)	ENSP00000343764.6:p.Val20310Met
ENST00000359218.10:c.41812G>A (TTN)	ENSP00000352154.5:p.Val13938Met
ENST00000359218.9:c.41812G>A (TTN)	ENSP00000352154.5:p.Val13938Met
ENST00000460472.6:c.41437G>A (TTN)	ENSP00000434586.1:p.Val13813Met
ENST00000591111.5:c.63709G>A (TTN)	ENSP00000465570.1:p.Val21237Met
ENST00000615779.4:c.63709G>A (TTN)	ENSP00000483597.1:p.Val21237Met
XM_011511729.1:c.67729G>A (TTN)	XP_011510031.1:p.Val22577Met
XM_011511730.1:c.41623G>A (TTN)	XP_011510032.1:p.Val13875Met
XM_011511731.1:c.41482G>A (TTN)	XP_011510033.1:p.Val13828Met
XM_017004819.1:c.67525G>A (TTN)	XP_016860308.1:p.Val22509Met
XM_017004820.1:c.62923G>A (TTN)	XP_016860309.1:p.Val20975Met
XM_017004821.1:c.62920G>A (TTN)	XP_016860310.1:p.Val20974Met
XM_017004822.1:c.59962G>A (TTN)	XP_016860311.1:p.Val19988Met
XM_017004823.1:c.41578G>A (TTN)	XP_016860312.1:p.Val13860Met
XM_024453094.1:c.63073G>A (TTN)	XP_024308862.1:p.Val21025Met
XM_024453095.1:c.63070G>A (TTN)	XP_024308863.1:p.Val21024Met
XM_024453096.1:c.62503G>A (TTN)	XP_024308864.1:p.Val20835Met
XM_024453097.1:c.59845G>A (TTN)	XP_024308865.1:p.Val19949Met
XM_024453098.1:c.59764G>A (TTN)	XP_024308866.1:p.Val19922Met
XM_024453099.1:c.41527G>A (TTN)	XP_024308867.1:p.Val13843Met
XM_024453100.1:c.31381G>A (TTN)	XP_024308868.1:p.Val10461Met