Canonical Allele Identifier: CA349419882

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178534931A>G , CM000664.2:g.178534931A>G	GRCh38
NC_000002.11:g.179399658A>G , CM000664.1:g.179399658A>G	GRCh37
NC_000002.10:g.179107904A>G	NCBI36
NG_011618.3:g.300872T>C , LRG_391:g.300872T>C
NG_051363.1:g.17105A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.101684T>C (TTN) MANE Select	NP_001254479.2:p.Ile33895Thr
ENST00000589042.5:c.101684T>C (TTN) MANE Select	ENSP00000467141.1:p.Ile33895Thr
NM_001256850.1:c.96761T>C (TTN)	NP_001243779.1:p.Ile32254Thr
NM_003319.4:c.74489T>C (TTN)	NP_003310.4:p.Ile24830Thr
NM_133378.4:c.93980T>C (TTN)	NP_596869.4:p.Ile31327Thr
NM_133432.3:c.74864T>C (TTN)	NP_597676.3:p.Ile24955Thr
NM_133437.4:c.75065T>C (TTN)	NP_597681.4:p.Ile25022Thr
NR_038271.1:n.446+11295A>G (TTN-AS1)
NR_038272.1:n.220-801A>G (TTN-AS1)
ENST00000342175.10:c.75065T>C (TTN)	ENSP00000340554.6:p.Ile25022Thr
ENST00000342175.11:c.75065T>C (TTN)	ENSP00000340554.6:p.Ile25022Thr
ENST00000342992.10:c.93980T>C (TTN)	ENSP00000343764.6:p.Ile31327Thr
ENST00000342992.11:c.93980T>C (TTN)	ENSP00000343764.6:p.Ile31327Thr
ENST00000359218.10:c.74864T>C (TTN)	ENSP00000352154.5:p.Ile24955Thr
ENST00000359218.9:c.74864T>C (TTN)	ENSP00000352154.5:p.Ile24955Thr
ENST00000460472.6:c.74489T>C (TTN)	ENSP00000434586.1:p.Ile24830Thr
ENST00000591111.5:c.96761T>C (TTN)	ENSP00000465570.1:p.Ile32254Thr
ENST00000615779.4:c.96761T>C (TTN)	ENSP00000483597.1:p.Ile32254Thr
XM_011511729.1:c.100781T>C (TTN)	XP_011510031.1:p.Ile33594Thr
XM_011511730.1:c.74675T>C (TTN)	XP_011510032.1:p.Ile24892Thr
XM_011511731.1:c.74534T>C (TTN)	XP_011510033.1:p.Ile24845Thr
XM_017004819.1:c.100577T>C (TTN)	XP_016860308.1:p.Ile33526Thr
XM_017004820.1:c.95975T>C (TTN)	XP_016860309.1:p.Ile31992Thr
XM_017004821.1:c.95972T>C (TTN)	XP_016860310.1:p.Ile31991Thr
XM_017004822.1:c.93014T>C (TTN)	XP_016860311.1:p.Ile31005Thr
XM_017004823.1:c.74630T>C (TTN)	XP_016860312.1:p.Ile24877Thr
XM_024453094.1:c.96125T>C (TTN)	XP_024308862.1:p.Ile32042Thr
XM_024453095.1:c.96122T>C (TTN)	XP_024308863.1:p.Ile32041Thr
XM_024453096.1:c.95555T>C (TTN)	XP_024308864.1:p.Ile31852Thr
XM_024453097.1:c.92897T>C (TTN)	XP_024308865.1:p.Ile30966Thr
XM_024453098.1:c.92816T>C (TTN)	XP_024308866.1:p.Ile30939Thr
XM_024453099.1:c.74579T>C (TTN)	XP_024308867.1:p.Ile24860Thr
XM_024453100.1:c.64433T>C (TTN)	XP_024308868.1:p.Ile21478Thr