Canonical Allele Identifier: CA349570333

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607940C>T , CM000664.2:g.178607940C>T	GRCh38
NC_000002.11:g.179472667C>T , CM000664.1:g.179472667C>T	GRCh37
NC_000002.10:g.179180912C>T	NCBI36
NG_011618.3:g.227863G>A , LRG_391:g.227863G>A
NG_051363.1:g.90114C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.52847G>A (TTN) MANE Select	NP_001254479.2:p.Trp17616Ter
ENST00000589042.5:c.52847G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp17616Ter
NM_001256850.1:c.47924G>A (TTN)	NP_001243779.1:p.Trp15975Ter
NM_003319.4:c.25652G>A (TTN)	NP_003310.4:p.Trp8551Ter
NM_133378.4:c.45143G>A (TTN)	NP_596869.4:p.Trp15048Ter
NM_133432.3:c.26027G>A (TTN)	NP_597676.3:p.Trp8676Ter
NM_133437.4:c.26228G>A (TTN)	NP_597681.4:p.Trp8743Ter
NR_038271.1:n.683-227C>T (TTN-AS1)
ENST00000342175.10:c.26228G>A (TTN)	ENSP00000340554.6:p.Trp8743Ter
ENST00000342175.11:c.26228G>A (TTN)	ENSP00000340554.6:p.Trp8743Ter
ENST00000342992.10:c.45143G>A (TTN)	ENSP00000343764.6:p.Trp15048Ter
ENST00000342992.11:c.45143G>A (TTN)	ENSP00000343764.6:p.Trp15048Ter
ENST00000359218.10:c.26027G>A (TTN)	ENSP00000352154.5:p.Trp8676Ter
ENST00000359218.9:c.26027G>A (TTN)	ENSP00000352154.5:p.Trp8676Ter
ENST00000460472.6:c.25652G>A (TTN)	ENSP00000434586.1:p.Trp8551Ter
ENST00000591111.5:c.47924G>A (TTN)	ENSP00000465570.1:p.Trp15975Ter
ENST00000615779.4:c.47924G>A (TTN)	ENSP00000483597.1:p.Trp15975Ter
XM_011511729.1:c.51944G>A (TTN)	XP_011510031.1:p.Trp17315Ter
XM_011511730.1:c.25838G>A (TTN)	XP_011510032.1:p.Trp8613Ter
XM_011511731.1:c.25697G>A (TTN)	XP_011510033.1:p.Trp8566Ter
XM_017004819.1:c.51740G>A (TTN)	XP_016860308.1:p.Trp17247Ter
XM_017004820.1:c.47138G>A (TTN)	XP_016860309.1:p.Trp15713Ter
XM_017004821.1:c.47135G>A (TTN)	XP_016860310.1:p.Trp15712Ter
XM_017004822.1:c.44177G>A (TTN)	XP_016860311.1:p.Trp14726Ter
XM_017004823.1:c.25793G>A (TTN)	XP_016860312.1:p.Trp8598Ter
XM_024453094.1:c.47288G>A (TTN)	XP_024308862.1:p.Trp15763Ter
XM_024453095.1:c.47285G>A (TTN)	XP_024308863.1:p.Trp15762Ter
XM_024453096.1:c.46718G>A (TTN)	XP_024308864.1:p.Trp15573Ter
XM_024453097.1:c.44060G>A (TTN)	XP_024308865.1:p.Trp14687Ter
XM_024453098.1:c.43979G>A (TTN)	XP_024308866.1:p.Trp14660Ter
XM_024453099.1:c.25742G>A (TTN)	XP_024308867.1:p.Trp8581Ter
XM_024453100.1:c.15596G>A (TTN)	XP_024308868.1:p.Trp5199Ter