Canonical Allele Identifier: CA1310521504

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544311G= , CM000664.2:g.178544311G=	GRCh38
NC_000002.11:g.179409038G= , CM000664.1:g.179409038G=	GRCh37
NC_000002.10:g.179117284G=	NCBI36
NG_011618.3:g.291492C= , LRG_391:g.291492C=
NG_051363.1:g.26485G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.88214C= (TTN)	ENSP00000343764.6:p.Pro29405=
ENST00000342175.11:c.69299C= (TTN)	ENSP00000340554.6:p.Pro23100=
ENST00000359218.10:c.69098C= (TTN)	ENSP00000352154.5:p.Pro23033=
ENST00000342175.10:c.69299C= (TTN)	ENSP00000340554.6:p.Pro23100=
ENST00000342992.10:c.88214C= (TTN)	ENSP00000343764.6:p.Pro29405=
ENST00000359218.9:c.69098C= (TTN)	ENSP00000352154.5:p.Pro23033=
ENST00000460472.6:c.68723C= (TTN)	ENSP00000434586.1:p.Pro22908=
ENST00000589042.5:c.95918C= (TTN) MANE Select	ENSP00000467141.1:p.Pro31973=
ENST00000591111.5:c.90995C= (TTN)	ENSP00000465570.1:p.Pro30332=
ENST00000615779.4:c.90995C= (TTN)	ENSP00000483597.1:p.Pro30332=
NM_001256850.1:c.90995C= (TTN)	NP_001243779.1:p.Pro30332=
NM_001267550.2:c.95918C= (TTN) MANE Select	NP_001254479.2:p.Pro31973=
NM_003319.4:c.68723C= (TTN)	NP_003310.4:p.Pro22908=
NM_133378.4:c.88214C= (TTN)	NP_596869.4:p.Pro29405=
NM_133432.3:c.69098C= (TTN)	NP_597676.3:p.Pro23033=
NM_133437.4:c.69299C= (TTN)	NP_597681.4:p.Pro23100=
NR_038271.1:n.446+20675G= (TTN-AS1)
NR_038272.1:n.2043+1950G= (TTN-AS1)
XM_011511729.1:c.95015C= (TTN)	XP_011510031.1:p.Pro31672=
XM_011511730.1:c.68909C= (TTN)	XP_011510032.1:p.Pro22970=
XM_011511731.1:c.68768C= (TTN)	XP_011510033.1:p.Pro22923=
XM_017004819.1:c.94811C= (TTN)	XP_016860308.1:p.Pro31604=
XM_017004820.1:c.90209C= (TTN)	XP_016860309.1:p.Pro30070=
XM_017004821.1:c.90206C= (TTN)	XP_016860310.1:p.Pro30069=
XM_017004822.1:c.87248C= (TTN)	XP_016860311.1:p.Pro29083=
XM_017004823.1:c.68864C= (TTN)	XP_016860312.1:p.Pro22955=
XM_024453094.1:c.90359C= (TTN)	XP_024308862.1:p.Pro30120=
XM_024453095.1:c.90356C= (TTN)	XP_024308863.1:p.Pro30119=
XM_024453096.1:c.89789C= (TTN)	XP_024308864.1:p.Pro29930=
XM_024453097.1:c.87131C= (TTN)	XP_024308865.1:p.Pro29044=
XM_024453098.1:c.87050C= (TTN)	XP_024308866.1:p.Pro29017=
XM_024453099.1:c.68813C= (TTN)	XP_024308867.1:p.Pro22938=
XM_024453100.1:c.58667C= (TTN)	XP_024308868.1:p.Pro19556=