Canonical Allele Identifier: CA1310549450

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614631C= , CM000664.2:g.178614631C=	GRCh38
NC_000002.11:g.179479358C= , CM000664.1:g.179479358C=	GRCh37
NC_000002.10:g.179187603C=	NCBI36
NG_011618.3:g.221172G= , LRG_391:g.221172G=
NG_051363.1:g.96805C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41179G= (TTN)	ENSP00000343764.6:p.Ala13727=
ENST00000342175.11:c.22264G= (TTN)	ENSP00000340554.6:p.Ala7422=
ENST00000359218.10:c.22063G= (TTN)	ENSP00000352154.5:p.Ala7355=
ENST00000342175.10:c.22264G= (TTN)	ENSP00000340554.6:p.Ala7422=
ENST00000342992.10:c.41179G= (TTN)	ENSP00000343764.6:p.Ala13727=
ENST00000359218.9:c.22063G= (TTN)	ENSP00000352154.5:p.Ala7355=
ENST00000460472.6:c.21688G= (TTN)	ENSP00000434586.1:p.Ala7230=
ENST00000589042.5:c.48883G= (TTN) MANE Select	ENSP00000467141.1:p.Ala16295=
ENST00000591111.5:c.43960G= (TTN)	ENSP00000465570.1:p.Ala14654=
ENST00000615779.4:c.43960G= (TTN)	ENSP00000483597.1:p.Ala14654=
NM_001256850.1:c.43960G= (TTN)	NP_001243779.1:p.Ala14654=
NM_001267550.2:c.48883G= (TTN) MANE Select	NP_001254479.2:p.Ala16295=
NM_003319.4:c.21688G= (TTN)	NP_003310.4:p.Ala7230=
NM_133378.4:c.41179G= (TTN)	NP_596869.4:p.Ala13727=
NM_133432.3:c.22063G= (TTN)	NP_597676.3:p.Ala7355=
NM_133437.4:c.22264G= (TTN)	NP_597681.4:p.Ala7422=
NR_038271.1:n.1379C= (TTN-AS1)
XM_011511729.1:c.47980G= (TTN)	XP_011510031.1:p.Ala15994=
XM_011511730.1:c.21874G= (TTN)	XP_011510032.1:p.Ala7292=
XM_011511731.1:c.21733G= (TTN)	XP_011510033.1:p.Ala7245=
XM_017004819.1:c.47776G= (TTN)	XP_016860308.1:p.Ala15926=
XM_017004820.1:c.43174G= (TTN)	XP_016860309.1:p.Ala14392=
XM_017004821.1:c.43171G= (TTN)	XP_016860310.1:p.Ala14391=
XM_017004822.1:c.40213G= (TTN)	XP_016860311.1:p.Ala13405=
XM_017004823.1:c.21829G= (TTN)	XP_016860312.1:p.Ala7277=
XM_024453094.1:c.43324G= (TTN)	XP_024308862.1:p.Ala14442=
XM_024453095.1:c.43321G= (TTN)	XP_024308863.1:p.Ala14441=
XM_024453096.1:c.42754G= (TTN)	XP_024308864.1:p.Ala14252=
XM_024453097.1:c.40096G= (TTN)	XP_024308865.1:p.Ala13366=
XM_024453098.1:c.40015G= (TTN)	XP_024308866.1:p.Ala13339=
XM_024453099.1:c.21778G= (TTN)	XP_024308867.1:p.Ala7260=
XM_024453100.1:c.11632G= (TTN)	XP_024308868.1:p.Ala3878=