Canonical Allele Identifier: CA1310521506

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544314A= , CM000664.2:g.178544314A=	GRCh38
NC_000002.11:g.179409041A= , CM000664.1:g.179409041A=	GRCh37
NC_000002.10:g.179117287A=	NCBI36
NG_011618.3:g.291489T= , LRG_391:g.291489T=
NG_051363.1:g.26488A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.88211T= (TTN)	ENSP00000343764.6:p.Val29404=
ENST00000342175.11:c.69296T= (TTN)	ENSP00000340554.6:p.Val23099=
ENST00000359218.10:c.69095T= (TTN)	ENSP00000352154.5:p.Val23032=
ENST00000342175.10:c.69296T= (TTN)	ENSP00000340554.6:p.Val23099=
ENST00000342992.10:c.88211T= (TTN)	ENSP00000343764.6:p.Val29404=
ENST00000359218.9:c.69095T= (TTN)	ENSP00000352154.5:p.Val23032=
ENST00000460472.6:c.68720T= (TTN)	ENSP00000434586.1:p.Val22907=
ENST00000589042.5:c.95915T= (TTN) MANE Select	ENSP00000467141.1:p.Val31972=
ENST00000591111.5:c.90992T= (TTN)	ENSP00000465570.1:p.Val30331=
ENST00000615779.4:c.90992T= (TTN)	ENSP00000483597.1:p.Val30331=
NM_001256850.1:c.90992T= (TTN)	NP_001243779.1:p.Val30331=
NM_001267550.2:c.95915T= (TTN) MANE Select	NP_001254479.2:p.Val31972=
NM_003319.4:c.68720T= (TTN)	NP_003310.4:p.Val22907=
NM_133378.4:c.88211T= (TTN)	NP_596869.4:p.Val29404=
NM_133432.3:c.69095T= (TTN)	NP_597676.3:p.Val23032=
NM_133437.4:c.69296T= (TTN)	NP_597681.4:p.Val23099=
NR_038271.1:n.446+20678A= (TTN-AS1)
NR_038272.1:n.2043+1953A= (TTN-AS1)
XM_011511729.1:c.95012T= (TTN)	XP_011510031.1:p.Val31671=
XM_011511730.1:c.68906T= (TTN)	XP_011510032.1:p.Val22969=
XM_011511731.1:c.68765T= (TTN)	XP_011510033.1:p.Val22922=
XM_017004819.1:c.94808T= (TTN)	XP_016860308.1:p.Val31603=
XM_017004820.1:c.90206T= (TTN)	XP_016860309.1:p.Val30069=
XM_017004821.1:c.90203T= (TTN)	XP_016860310.1:p.Val30068=
XM_017004822.1:c.87245T= (TTN)	XP_016860311.1:p.Val29082=
XM_017004823.1:c.68861T= (TTN)	XP_016860312.1:p.Val22954=
XM_024453094.1:c.90356T= (TTN)	XP_024308862.1:p.Val30119=
XM_024453095.1:c.90353T= (TTN)	XP_024308863.1:p.Val30118=
XM_024453096.1:c.89786T= (TTN)	XP_024308864.1:p.Val29929=
XM_024453097.1:c.87128T= (TTN)	XP_024308865.1:p.Val29043=
XM_024453098.1:c.87047T= (TTN)	XP_024308866.1:p.Val29016=
XM_024453099.1:c.68810T= (TTN)	XP_024308867.1:p.Val22937=
XM_024453100.1:c.58664T= (TTN)	XP_024308868.1:p.Val19555=