Canonical Allele Identifier: CA349607190

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614537G>T , CM000664.2:g.178614537G>T	GRCh38
NC_000002.11:g.179479264G>T , CM000664.1:g.179479264G>T	GRCh37
NC_000002.10:g.179187509G>T	NCBI36
NG_011618.3:g.221266C>A , LRG_391:g.221266C>A
NG_051363.1:g.96711G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.48977C>A (TTN) MANE Select	NP_001254479.2:p.Thr16326Asn
ENST00000589042.5:c.48977C>A (TTN) MANE Select	ENSP00000467141.1:p.Thr16326Asn
NM_001256850.1:c.44054C>A (TTN)	NP_001243779.1:p.Thr14685Asn
NM_003319.4:c.21782C>A (TTN)	NP_003310.4:p.Thr7261Asn
NM_133378.4:c.41273C>A (TTN)	NP_596869.4:p.Thr13758Asn
NM_133432.3:c.22157C>A (TTN)	NP_597676.3:p.Thr7386Asn
NM_133437.4:c.22358C>A (TTN)	NP_597681.4:p.Thr7453Asn
NR_038271.1:n.1285G>T (TTN-AS1)
ENST00000342175.10:c.22358C>A (TTN)	ENSP00000340554.6:p.Thr7453Asn
ENST00000342175.11:c.22358C>A (TTN)	ENSP00000340554.6:p.Thr7453Asn
ENST00000342992.10:c.41273C>A (TTN)	ENSP00000343764.6:p.Thr13758Asn
ENST00000342992.11:c.41273C>A (TTN)	ENSP00000343764.6:p.Thr13758Asn
ENST00000359218.10:c.22157C>A (TTN)	ENSP00000352154.5:p.Thr7386Asn
ENST00000359218.9:c.22157C>A (TTN)	ENSP00000352154.5:p.Thr7386Asn
ENST00000460472.6:c.21782C>A (TTN)	ENSP00000434586.1:p.Thr7261Asn
ENST00000591111.5:c.44054C>A (TTN)	ENSP00000465570.1:p.Thr14685Asn
ENST00000615779.4:c.44054C>A (TTN)	ENSP00000483597.1:p.Thr14685Asn
XM_011511729.1:c.48074C>A (TTN)	XP_011510031.1:p.Thr16025Asn
XM_011511730.1:c.21968C>A (TTN)	XP_011510032.1:p.Thr7323Asn
XM_011511731.1:c.21827C>A (TTN)	XP_011510033.1:p.Thr7276Asn
XM_017004819.1:c.47870C>A (TTN)	XP_016860308.1:p.Thr15957Asn
XM_017004820.1:c.43268C>A (TTN)	XP_016860309.1:p.Thr14423Asn
XM_017004821.1:c.43265C>A (TTN)	XP_016860310.1:p.Thr14422Asn
XM_017004822.1:c.40307C>A (TTN)	XP_016860311.1:p.Thr13436Asn
XM_017004823.1:c.21923C>A (TTN)	XP_016860312.1:p.Thr7308Asn
XM_024453094.1:c.43418C>A (TTN)	XP_024308862.1:p.Thr14473Asn
XM_024453095.1:c.43415C>A (TTN)	XP_024308863.1:p.Thr14472Asn
XM_024453096.1:c.42848C>A (TTN)	XP_024308864.1:p.Thr14283Asn
XM_024453097.1:c.40190C>A (TTN)	XP_024308865.1:p.Thr13397Asn
XM_024453098.1:c.40109C>A (TTN)	XP_024308866.1:p.Thr13370Asn
XM_024453099.1:c.21872C>A (TTN)	XP_024308867.1:p.Thr7291Asn
XM_024453100.1:c.11726C>A (TTN)	XP_024308868.1:p.Thr3909Asn