Canonical Allele Identifier: CA349540667

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178558570C>T , CM000664.2:g.178558570C>T	GRCh38
NC_000002.11:g.179423297C>T , CM000664.1:g.179423297C>T	GRCh37
NC_000002.10:g.179131543C>T	NCBI36
NG_011618.3:g.277233G>A , LRG_391:g.277233G>A
NG_051363.1:g.40744C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.86889G>A (TTN) MANE Select	NP_001254479.2:p.Trp28963Ter
ENST00000589042.5:c.86889G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp28963Ter
NM_001256850.1:c.81966G>A (TTN)	NP_001243779.1:p.Trp27322Ter
NM_003319.4:c.59694G>A (TTN)	NP_003310.4:p.Trp19898Ter
NM_133378.4:c.79185G>A (TTN)	NP_596869.4:p.Trp26395Ter
NM_133432.3:c.60069G>A (TTN)	NP_597676.3:p.Trp20023Ter
NM_133437.4:c.60270G>A (TTN)	NP_597681.4:p.Trp20090Ter
NR_038271.1:n.447-12730C>T (TTN-AS1)
NR_038272.1:n.2043+16209C>T (TTN-AS1)
ENST00000342175.10:c.60270G>A (TTN)	ENSP00000340554.6:p.Trp20090Ter
ENST00000342175.11:c.60270G>A (TTN)	ENSP00000340554.6:p.Trp20090Ter
ENST00000342992.10:c.79185G>A (TTN)	ENSP00000343764.6:p.Trp26395Ter
ENST00000342992.11:c.79185G>A (TTN)	ENSP00000343764.6:p.Trp26395Ter
ENST00000359218.10:c.60069G>A (TTN)	ENSP00000352154.5:p.Trp20023Ter
ENST00000359218.9:c.60069G>A (TTN)	ENSP00000352154.5:p.Trp20023Ter
ENST00000460472.6:c.59694G>A (TTN)	ENSP00000434586.1:p.Trp19898Ter
ENST00000591111.5:c.81966G>A (TTN)	ENSP00000465570.1:p.Trp27322Ter
ENST00000615779.4:c.81966G>A (TTN)	ENSP00000483597.1:p.Trp27322Ter
XM_011511729.1:c.85986G>A (TTN)	XP_011510031.1:p.Trp28662Ter
XM_011511730.1:c.59880G>A (TTN)	XP_011510032.1:p.Trp19960Ter
XM_011511731.1:c.59739G>A (TTN)	XP_011510033.1:p.Trp19913Ter
XM_017004819.1:c.85782G>A (TTN)	XP_016860308.1:p.Trp28594Ter
XM_017004820.1:c.81180G>A (TTN)	XP_016860309.1:p.Trp27060Ter
XM_017004821.1:c.81177G>A (TTN)	XP_016860310.1:p.Trp27059Ter
XM_017004822.1:c.78219G>A (TTN)	XP_016860311.1:p.Trp26073Ter
XM_017004823.1:c.59835G>A (TTN)	XP_016860312.1:p.Trp19945Ter
XM_024453094.1:c.81330G>A (TTN)	XP_024308862.1:p.Trp27110Ter
XM_024453095.1:c.81327G>A (TTN)	XP_024308863.1:p.Trp27109Ter
XM_024453096.1:c.80760G>A (TTN)	XP_024308864.1:p.Trp26920Ter
XM_024453097.1:c.78102G>A (TTN)	XP_024308865.1:p.Trp26034Ter
XM_024453098.1:c.78021G>A (TTN)	XP_024308866.1:p.Trp26007Ter
XM_024453099.1:c.59784G>A (TTN)	XP_024308867.1:p.Trp19928Ter
XM_024453100.1:c.49638G>A (TTN)	XP_024308868.1:p.Trp16546Ter