Canonical Allele Identifier: CA1310514491

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527491G= , CM000664.2:g.178527491G=	GRCh38
NC_000002.11:g.179392218G= , CM000664.1:g.179392218G=	GRCh37
NC_000002.10:g.179100464G=	NCBI36
NG_011618.3:g.308312C= , LRG_391:g.308312C=
NG_051363.1:g.9665G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.99931C= (TTN)	ENSP00000343764.6:p.Gln33311=
ENST00000342175.11:c.81016C= (TTN)	ENSP00000340554.6:p.Gln27006=
ENST00000359218.10:c.80815C= (TTN)	ENSP00000352154.5:p.Gln26939=
ENST00000342175.10:c.81016C= (TTN)	ENSP00000340554.6:p.Gln27006=
ENST00000342992.10:c.99931C= (TTN)	ENSP00000343764.6:p.Gln33311=
ENST00000359218.9:c.80815C= (TTN)	ENSP00000352154.5:p.Gln26939=
ENST00000460472.6:c.80440C= (TTN)	ENSP00000434586.1:p.Gln26814=
ENST00000589042.5:c.107635C= (TTN) MANE Select	ENSP00000467141.1:p.Gln35879=
ENST00000591111.5:c.102712C= (TTN)	ENSP00000465570.1:p.Gln34238=
ENST00000615779.4:c.102712C= (TTN)	ENSP00000483597.1:p.Gln34238=
NM_001256850.1:c.102712C= (TTN)	NP_001243779.1:p.Gln34238=
NM_001267550.2:c.107635C= (TTN) MANE Select	NP_001254479.2:p.Gln35879=
NM_003319.4:c.80440C= (TTN)	NP_003310.4:p.Gln26814=
NM_133378.4:c.99931C= (TTN)	NP_596869.4:p.Gln33311=
NM_133432.3:c.80815C= (TTN)	NP_597676.3:p.Gln26939=
NM_133437.4:c.81016C= (TTN)	NP_597681.4:p.Gln27006=
NR_038271.1:n.446+3855G= (TTN-AS1)
NR_038272.1:n.219+3855G= (TTN-AS1)
XM_011511729.1:c.106732C= (TTN)	XP_011510031.1:p.Gln35578=
XM_011511730.1:c.80626C= (TTN)	XP_011510032.1:p.Gln26876=
XM_011511731.1:c.80485C= (TTN)	XP_011510033.1:p.Gln26829=
XM_017004819.1:c.106528C= (TTN)	XP_016860308.1:p.Gln35510=
XM_017004820.1:c.101926C= (TTN)	XP_016860309.1:p.Gln33976=
XM_017004821.1:c.101923C= (TTN)	XP_016860310.1:p.Gln33975=
XM_017004822.1:c.98965C= (TTN)	XP_016860311.1:p.Gln32989=
XM_017004823.1:c.80581C= (TTN)	XP_016860312.1:p.Gln26861=
XM_024453094.1:c.102076C= (TTN)	XP_024308862.1:p.Gln34026=
XM_024453095.1:c.102073C= (TTN)	XP_024308863.1:p.Gln34025=
XM_024453096.1:c.101506C= (TTN)	XP_024308864.1:p.Gln33836=
XM_024453097.1:c.98848C= (TTN)	XP_024308865.1:p.Gln32950=
XM_024453098.1:c.98767C= (TTN)	XP_024308866.1:p.Gln32923=
XM_024453099.1:c.80530C= (TTN)	XP_024308867.1:p.Gln26844=
XM_024453100.1:c.70384C= (TTN)	XP_024308868.1:p.Gln23462=