Canonical Allele Identifier: CA1310523391

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546774C= , CM000664.2:g.178546774C=	GRCh38
NC_000002.11:g.179411501C= , CM000664.1:g.179411501C=	GRCh37
NC_000002.10:g.179119747C=	NCBI36
NG_011618.3:g.289029G= , LRG_391:g.289029G=
NG_051363.1:g.28948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86950G= (TTN)	ENSP00000343764.6:p.Gly28984=
ENST00000342175.11:c.68035G= (TTN)	ENSP00000340554.6:p.Gly22679=
ENST00000359218.10:c.67834G= (TTN)	ENSP00000352154.5:p.Gly22612=
ENST00000342175.10:c.68035G= (TTN)	ENSP00000340554.6:p.Gly22679=
ENST00000342992.10:c.86950G= (TTN)	ENSP00000343764.6:p.Gly28984=
ENST00000359218.9:c.67834G= (TTN)	ENSP00000352154.5:p.Gly22612=
ENST00000460472.6:c.67459G= (TTN)	ENSP00000434586.1:p.Gly22487=
ENST00000589042.5:c.94654G= (TTN) MANE Select	ENSP00000467141.1:p.Gly31552=
ENST00000591111.5:c.89731G= (TTN)	ENSP00000465570.1:p.Gly29911=
ENST00000615779.4:c.89731G= (TTN)	ENSP00000483597.1:p.Gly29911=
NM_001256850.1:c.89731G= (TTN)	NP_001243779.1:p.Gly29911=
NM_001267550.2:c.94654G= (TTN) MANE Select	NP_001254479.2:p.Gly31552=
NM_003319.4:c.67459G= (TTN)	NP_003310.4:p.Gly22487=
NM_133378.4:c.86950G= (TTN)	NP_596869.4:p.Gly28984=
NM_133432.3:c.67834G= (TTN)	NP_597676.3:p.Gly22612=
NM_133437.4:c.68035G= (TTN)	NP_597681.4:p.Gly22679=
NR_038271.1:n.446+23138C= (TTN-AS1)
NR_038272.1:n.2043+4413C= (TTN-AS1)
XM_011511729.1:c.93751G= (TTN)	XP_011510031.1:p.Gly31251=
XM_011511730.1:c.67645G= (TTN)	XP_011510032.1:p.Gly22549=
XM_011511731.1:c.67504G= (TTN)	XP_011510033.1:p.Gly22502=
XM_017004819.1:c.93547G= (TTN)	XP_016860308.1:p.Gly31183=
XM_017004820.1:c.88945G= (TTN)	XP_016860309.1:p.Gly29649=
XM_017004821.1:c.88942G= (TTN)	XP_016860310.1:p.Gly29648=
XM_017004822.1:c.85984G= (TTN)	XP_016860311.1:p.Gly28662=
XM_017004823.1:c.67600G= (TTN)	XP_016860312.1:p.Gly22534=
XM_024453094.1:c.89095G= (TTN)	XP_024308862.1:p.Gly29699=
XM_024453095.1:c.89092G= (TTN)	XP_024308863.1:p.Gly29698=
XM_024453096.1:c.88525G= (TTN)	XP_024308864.1:p.Gly29509=
XM_024453097.1:c.85867G= (TTN)	XP_024308865.1:p.Gly28623=
XM_024453098.1:c.85786G= (TTN)	XP_024308866.1:p.Gly28596=
XM_024453099.1:c.67549G= (TTN)	XP_024308867.1:p.Gly22517=
XM_024453100.1:c.57403G= (TTN)	XP_024308868.1:p.Gly19135=