Canonical Allele Identifier: CA1310537082

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584573G= , CM000664.2:g.178584573G=	GRCh38
NC_000002.11:g.179449300G= , CM000664.1:g.179449300G=	GRCh37
NC_000002.10:g.179157546G=	NCBI36
NG_011618.3:g.251230C= , LRG_391:g.251230C=
NG_051363.1:g.66747G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.57274C= (TTN)	ENSP00000343764.6:p.Pro19092=
ENST00000342175.11:c.38359C= (TTN)	ENSP00000340554.6:p.Pro12787=
ENST00000359218.10:c.38158C= (TTN)	ENSP00000352154.5:p.Pro12720=
ENST00000342175.10:c.38359C= (TTN)	ENSP00000340554.6:p.Pro12787=
ENST00000342992.10:c.57274C= (TTN)	ENSP00000343764.6:p.Pro19092=
ENST00000359218.9:c.38158C= (TTN)	ENSP00000352154.5:p.Pro12720=
ENST00000460472.6:c.37783C= (TTN)	ENSP00000434586.1:p.Pro12595=
ENST00000589042.5:c.64978C= (TTN) MANE Select	ENSP00000467141.1:p.Pro21660=
ENST00000591111.5:c.60055C= (TTN)	ENSP00000465570.1:p.Pro20019=
ENST00000615779.4:c.60055C= (TTN)	ENSP00000483597.1:p.Pro20019=
NM_001256850.1:c.60055C= (TTN)	NP_001243779.1:p.Pro20019=
NM_001267550.2:c.64978C= (TTN) MANE Select	NP_001254479.2:p.Pro21660=
NM_003319.4:c.37783C= (TTN)	NP_003310.4:p.Pro12595=
NM_133378.4:c.57274C= (TTN)	NP_596869.4:p.Pro19092=
NM_133432.3:c.38158C= (TTN)	NP_597676.3:p.Pro12720=
NM_133437.4:c.38359C= (TTN)	NP_597681.4:p.Pro12787=
NR_038271.1:n.597-13023G= (TTN-AS1)
NR_038272.1:n.2768G= (TTN-AS1)
XM_011511729.1:c.64075C= (TTN)	XP_011510031.1:p.Pro21359=
XM_011511730.1:c.37969C= (TTN)	XP_011510032.1:p.Pro12657=
XM_011511731.1:c.37828C= (TTN)	XP_011510033.1:p.Pro12610=
XM_017004819.1:c.63871C= (TTN)	XP_016860308.1:p.Pro21291=
XM_017004820.1:c.59269C= (TTN)	XP_016860309.1:p.Pro19757=
XM_017004821.1:c.59266C= (TTN)	XP_016860310.1:p.Pro19756=
XM_017004822.1:c.56308C= (TTN)	XP_016860311.1:p.Pro18770=
XM_017004823.1:c.37924C= (TTN)	XP_016860312.1:p.Pro12642=
XM_024453094.1:c.59419C= (TTN)	XP_024308862.1:p.Pro19807=
XM_024453095.1:c.59416C= (TTN)	XP_024308863.1:p.Pro19806=
XM_024453096.1:c.58849C= (TTN)	XP_024308864.1:p.Pro19617=
XM_024453097.1:c.56191C= (TTN)	XP_024308865.1:p.Pro18731=
XM_024453098.1:c.56110C= (TTN)	XP_024308866.1:p.Pro18704=
XM_024453099.1:c.37873C= (TTN)	XP_024308867.1:p.Pro12625=
XM_024453100.1:c.27727C= (TTN)	XP_024308868.1:p.Pro9243=