Canonical Allele Identifier: CA1310518109

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532167C= , CM000664.2:g.178532167C=	GRCh38
NC_000002.11:g.179396894C= , CM000664.1:g.179396894C=	GRCh37
NC_000002.10:g.179105140C=	NCBI36
NG_011618.3:g.303636G= , LRG_391:g.303636G=
NG_051363.1:g.14341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96744G= (TTN)	ENSP00000343764.6:p.Glu32248=
ENST00000342175.11:c.77829G= (TTN)	ENSP00000340554.6:p.Glu25943=
ENST00000359218.10:c.77628G= (TTN)	ENSP00000352154.5:p.Glu25876=
ENST00000342175.10:c.77829G= (TTN)	ENSP00000340554.6:p.Glu25943=
ENST00000342992.10:c.96744G= (TTN)	ENSP00000343764.6:p.Glu32248=
ENST00000359218.9:c.77628G= (TTN)	ENSP00000352154.5:p.Glu25876=
ENST00000460472.6:c.77253G= (TTN)	ENSP00000434586.1:p.Glu25751=
ENST00000589042.5:c.104448G= (TTN) MANE Select	ENSP00000467141.1:p.Glu34816=
ENST00000591111.5:c.99525G= (TTN)	ENSP00000465570.1:p.Glu33175=
ENST00000615779.4:c.99525G= (TTN)	ENSP00000483597.1:p.Glu33175=
NM_001256850.1:c.99525G= (TTN)	NP_001243779.1:p.Glu33175=
NM_001267550.2:c.104448G= (TTN) MANE Select	NP_001254479.2:p.Glu34816=
NM_003319.4:c.77253G= (TTN)	NP_003310.4:p.Glu25751=
NM_133378.4:c.96744G= (TTN)	NP_596869.4:p.Glu32248=
NM_133432.3:c.77628G= (TTN)	NP_597676.3:p.Glu25876=
NM_133437.4:c.77829G= (TTN)	NP_597681.4:p.Glu25943=
NR_038271.1:n.446+8531C= (TTN-AS1)
NR_038272.1:n.220-3565C= (TTN-AS1)
XM_011511729.1:c.103545G= (TTN)	XP_011510031.1:p.Glu34515=
XM_011511730.1:c.77439G= (TTN)	XP_011510032.1:p.Glu25813=
XM_011511731.1:c.77298G= (TTN)	XP_011510033.1:p.Glu25766=
XM_017004819.1:c.103341G= (TTN)	XP_016860308.1:p.Glu34447=
XM_017004820.1:c.98739G= (TTN)	XP_016860309.1:p.Glu32913=
XM_017004821.1:c.98736G= (TTN)	XP_016860310.1:p.Glu32912=
XM_017004822.1:c.95778G= (TTN)	XP_016860311.1:p.Glu31926=
XM_017004823.1:c.77394G= (TTN)	XP_016860312.1:p.Glu25798=
XM_024453094.1:c.98889G= (TTN)	XP_024308862.1:p.Glu32963=
XM_024453095.1:c.98886G= (TTN)	XP_024308863.1:p.Glu32962=
XM_024453096.1:c.98319G= (TTN)	XP_024308864.1:p.Glu32773=
XM_024453097.1:c.95661G= (TTN)	XP_024308865.1:p.Glu31887=
XM_024453098.1:c.95580G= (TTN)	XP_024308866.1:p.Glu31860=
XM_024453099.1:c.77343G= (TTN)	XP_024308867.1:p.Glu25781=
XM_024453100.1:c.67197G= (TTN)	XP_024308868.1:p.Glu22399=