Canonical Allele Identifier: CA349492946

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549100C>T , CM000664.2:g.178549100C>T	GRCh38
NC_000002.11:g.179413827C>T , CM000664.1:g.179413827C>T	GRCh37
NC_000002.10:g.179122073C>T	NCBI36
NG_011618.3:g.286703G>A , LRG_391:g.286703G>A
NG_051363.1:g.31274C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.92526G>A (TTN) MANE Select	NP_001254479.2:p.Trp30842Ter
ENST00000589042.5:c.92526G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp30842Ter
NM_001256850.1:c.87603G>A (TTN)	NP_001243779.1:p.Trp29201Ter
NM_003319.4:c.65331G>A (TTN)	NP_003310.4:p.Trp21777Ter
NM_133378.4:c.84822G>A (TTN)	NP_596869.4:p.Trp28274Ter
NM_133432.3:c.65706G>A (TTN)	NP_597676.3:p.Trp21902Ter
NM_133437.4:c.65907G>A (TTN)	NP_597681.4:p.Trp21969Ter
NR_038271.1:n.447-22200C>T (TTN-AS1)
NR_038272.1:n.2043+6739C>T (TTN-AS1)
ENST00000342175.10:c.65907G>A (TTN)	ENSP00000340554.6:p.Trp21969Ter
ENST00000342175.11:c.65907G>A (TTN)	ENSP00000340554.6:p.Trp21969Ter
ENST00000342992.10:c.84822G>A (TTN)	ENSP00000343764.6:p.Trp28274Ter
ENST00000342992.11:c.84822G>A (TTN)	ENSP00000343764.6:p.Trp28274Ter
ENST00000359218.10:c.65706G>A (TTN)	ENSP00000352154.5:p.Trp21902Ter
ENST00000359218.9:c.65706G>A (TTN)	ENSP00000352154.5:p.Trp21902Ter
ENST00000460472.6:c.65331G>A (TTN)	ENSP00000434586.1:p.Trp21777Ter
ENST00000591111.5:c.87603G>A (TTN)	ENSP00000465570.1:p.Trp29201Ter
ENST00000615779.4:c.87603G>A (TTN)	ENSP00000483597.1:p.Trp29201Ter
XM_011511729.1:c.91623G>A (TTN)	XP_011510031.1:p.Trp30541Ter
XM_011511730.1:c.65517G>A (TTN)	XP_011510032.1:p.Trp21839Ter
XM_011511731.1:c.65376G>A (TTN)	XP_011510033.1:p.Trp21792Ter
XM_017004819.1:c.91419G>A (TTN)	XP_016860308.1:p.Trp30473Ter
XM_017004820.1:c.86817G>A (TTN)	XP_016860309.1:p.Trp28939Ter
XM_017004821.1:c.86814G>A (TTN)	XP_016860310.1:p.Trp28938Ter
XM_017004822.1:c.83856G>A (TTN)	XP_016860311.1:p.Trp27952Ter
XM_017004823.1:c.65472G>A (TTN)	XP_016860312.1:p.Trp21824Ter
XM_024453094.1:c.86967G>A (TTN)	XP_024308862.1:p.Trp28989Ter
XM_024453095.1:c.86964G>A (TTN)	XP_024308863.1:p.Trp28988Ter
XM_024453096.1:c.86397G>A (TTN)	XP_024308864.1:p.Trp28799Ter
XM_024453097.1:c.83739G>A (TTN)	XP_024308865.1:p.Trp27913Ter
XM_024453098.1:c.83658G>A (TTN)	XP_024308866.1:p.Trp27886Ter
XM_024453099.1:c.65421G>A (TTN)	XP_024308867.1:p.Trp21807Ter
XM_024453100.1:c.55275G>A (TTN)	XP_024308868.1:p.Trp18425Ter