Canonical Allele Identifier: CA1310537541

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586611G= , CM000664.2:g.178586611G=	GRCh38
NC_000002.11:g.179451338G= , CM000664.1:g.179451338G=	GRCh37
NC_000002.10:g.179159584G=	NCBI36
NG_011618.3:g.249192C= , LRG_391:g.249192C=
NG_051363.1:g.68785G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.56586C= (TTN)	ENSP00000343764.6:p.Gly18862=
ENST00000342175.11:c.37671C= (TTN)	ENSP00000340554.6:p.Gly12557=
ENST00000359218.10:c.37470C= (TTN)	ENSP00000352154.5:p.Gly12490=
ENST00000342175.10:c.37671C= (TTN)	ENSP00000340554.6:p.Gly12557=
ENST00000342992.10:c.56586C= (TTN)	ENSP00000343764.6:p.Gly18862=
ENST00000359218.9:c.37470C= (TTN)	ENSP00000352154.5:p.Gly12490=
ENST00000460472.6:c.37095C= (TTN)	ENSP00000434586.1:p.Gly12365=
ENST00000589042.5:c.64290C= (TTN) MANE Select	ENSP00000467141.1:p.Gly21430=
ENST00000591111.5:c.59367C= (TTN)	ENSP00000465570.1:p.Gly19789=
ENST00000615779.4:c.59367C= (TTN)	ENSP00000483597.1:p.Gly19789=
NM_001256850.1:c.59367C= (TTN)	NP_001243779.1:p.Gly19789=
NM_001267550.2:c.64290C= (TTN) MANE Select	NP_001254479.2:p.Gly21430=
NM_003319.4:c.37095C= (TTN)	NP_003310.4:p.Gly12365=
NM_133378.4:c.56586C= (TTN)	NP_596869.4:p.Gly18862=
NM_133432.3:c.37470C= (TTN)	NP_597676.3:p.Gly12490=
NM_133437.4:c.37671C= (TTN)	NP_597681.4:p.Gly12557=
NR_038271.1:n.597-10985G= (TTN-AS1)
NR_038272.1:n.3188+1618G= (TTN-AS1)
XM_011511729.1:c.63387C= (TTN)	XP_011510031.1:p.Gly21129=
XM_011511730.1:c.37281C= (TTN)	XP_011510032.1:p.Gly12427=
XM_011511731.1:c.37140C= (TTN)	XP_011510033.1:p.Gly12380=
XM_017004819.1:c.63183C= (TTN)	XP_016860308.1:p.Gly21061=
XM_017004820.1:c.58581C= (TTN)	XP_016860309.1:p.Gly19527=
XM_017004821.1:c.58578C= (TTN)	XP_016860310.1:p.Gly19526=
XM_017004822.1:c.55620C= (TTN)	XP_016860311.1:p.Gly18540=
XM_017004823.1:c.37236C= (TTN)	XP_016860312.1:p.Gly12412=
XM_024453094.1:c.58731C= (TTN)	XP_024308862.1:p.Gly19577=
XM_024453095.1:c.58728C= (TTN)	XP_024308863.1:p.Gly19576=
XM_024453096.1:c.58161C= (TTN)	XP_024308864.1:p.Gly19387=
XM_024453097.1:c.55503C= (TTN)	XP_024308865.1:p.Gly18501=
XM_024453098.1:c.55422C= (TTN)	XP_024308866.1:p.Gly18474=
XM_024453099.1:c.37185C= (TTN)	XP_024308867.1:p.Gly12395=
XM_024453100.1:c.27039C= (TTN)	XP_024308868.1:p.Gly9013=