Canonical Allele Identifier: CA1984868

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527156C>T , CM000664.2:g.178527156C>T	GRCh38
NC_000002.11:g.179391883C>T , CM000664.1:g.179391883C>T	GRCh37
NC_000002.10:g.179100129C>T	NCBI36
NG_011618.3:g.308647G>A , LRG_391:g.308647G>A
NG_051363.1:g.9330C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107832G>A (TTN) MANE Select	NP_001254479.2:p.Arg35944=
ENST00000589042.5:c.107832G>A (TTN) MANE Select	ENSP00000467141.1:p.Arg35944=
NM_001256850.1:c.102909G>A (TTN)	NP_001243779.1:p.Arg34303=
NM_003319.4:c.80637G>A (TTN)	NP_003310.4:p.Arg26879=
NM_133378.4:c.100128G>A (TTN)	NP_596869.4:p.Arg33376=
NM_133432.3:c.81012G>A (TTN)	NP_597676.3:p.Arg27004=
NM_133437.4:c.81213G>A (TTN)	NP_597681.4:p.Arg27071=
NR_038271.1:n.446+3520C>T (TTN-AS1)
NR_038272.1:n.219+3520C>T (TTN-AS1)
ENST00000342175.10:c.81213G>A (TTN)	ENSP00000340554.6:p.Arg27071=
ENST00000342175.11:c.81213G>A (TTN)	ENSP00000340554.6:p.Arg27071=
ENST00000342992.10:c.100128G>A (TTN)	ENSP00000343764.6:p.Arg33376=
ENST00000342992.11:c.100128G>A (TTN)	ENSP00000343764.6:p.Arg33376=
ENST00000359218.10:c.81012G>A (TTN)	ENSP00000352154.5:p.Arg27004=
ENST00000359218.9:c.81012G>A (TTN)	ENSP00000352154.5:p.Arg27004=
ENST00000460472.6:c.80637G>A (TTN)	ENSP00000434586.1:p.Arg26879=
ENST00000591111.5:c.102909G>A (TTN)	ENSP00000465570.1:p.Arg34303=
ENST00000615779.4:c.102909G>A (TTN)	ENSP00000483597.1:p.Arg34303=
XM_011511729.1:c.106929G>A (TTN)	XP_011510031.1:p.Arg35643=
XM_011511730.1:c.80823G>A (TTN)	XP_011510032.1:p.Arg26941=
XM_011511731.1:c.80682G>A (TTN)	XP_011510033.1:p.Arg26894=
XM_017004819.1:c.106725G>A (TTN)	XP_016860308.1:p.Arg35575=
XM_017004820.1:c.102123G>A (TTN)	XP_016860309.1:p.Arg34041=
XM_017004821.1:c.102120G>A (TTN)	XP_016860310.1:p.Arg34040=
XM_017004822.1:c.99162G>A (TTN)	XP_016860311.1:p.Arg33054=
XM_017004823.1:c.80778G>A (TTN)	XP_016860312.1:p.Arg26926=
XM_024453094.1:c.102273G>A (TTN)	XP_024308862.1:p.Arg34091=
XM_024453095.1:c.102270G>A (TTN)	XP_024308863.1:p.Arg34090=
XM_024453096.1:c.101703G>A (TTN)	XP_024308864.1:p.Arg33901=
XM_024453097.1:c.99045G>A (TTN)	XP_024308865.1:p.Arg33015=
XM_024453098.1:c.98964G>A (TTN)	XP_024308866.1:p.Arg32988=
XM_024453099.1:c.80727G>A (TTN)	XP_024308867.1:p.Arg26909=
XM_024453100.1:c.70581G>A (TTN)	XP_024308868.1:p.Arg23527=