Canonical Allele Identifier: CA349559104

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178561530C>T , CM000664.2:g.178561530C>T	GRCh38
NC_000002.11:g.179426257C>T , CM000664.1:g.179426257C>T	GRCh37
NC_000002.10:g.179134503C>T	NCBI36
NG_011618.3:g.274273G>A , LRG_391:g.274273G>A
NG_051363.1:g.43704C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.84602G>A (TTN) MANE Select	NP_001254479.2:p.Trp28201Ter
ENST00000589042.5:c.84602G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp28201Ter
NM_001256850.1:c.79679G>A (TTN)	NP_001243779.1:p.Trp26560Ter
NM_003319.4:c.57407G>A (TTN)	NP_003310.4:p.Trp19136Ter
NM_133378.4:c.76898G>A (TTN)	NP_596869.4:p.Trp25633Ter
NM_133432.3:c.57782G>A (TTN)	NP_597676.3:p.Trp19261Ter
NM_133437.4:c.57983G>A (TTN)	NP_597681.4:p.Trp19328Ter
NR_038271.1:n.447-9770C>T (TTN-AS1)
NR_038272.1:n.2043+19169C>T (TTN-AS1)
ENST00000342175.10:c.57983G>A (TTN)	ENSP00000340554.6:p.Trp19328Ter
ENST00000342175.11:c.57983G>A (TTN)	ENSP00000340554.6:p.Trp19328Ter
ENST00000342992.10:c.76898G>A (TTN)	ENSP00000343764.6:p.Trp25633Ter
ENST00000342992.11:c.76898G>A (TTN)	ENSP00000343764.6:p.Trp25633Ter
ENST00000359218.10:c.57782G>A (TTN)	ENSP00000352154.5:p.Trp19261Ter
ENST00000359218.9:c.57782G>A (TTN)	ENSP00000352154.5:p.Trp19261Ter
ENST00000460472.6:c.57407G>A (TTN)	ENSP00000434586.1:p.Trp19136Ter
ENST00000591111.5:c.79679G>A (TTN)	ENSP00000465570.1:p.Trp26560Ter
ENST00000615779.4:c.79679G>A (TTN)	ENSP00000483597.1:p.Trp26560Ter
XM_011511729.1:c.83699G>A (TTN)	XP_011510031.1:p.Trp27900Ter
XM_011511730.1:c.57593G>A (TTN)	XP_011510032.1:p.Trp19198Ter
XM_011511731.1:c.57452G>A (TTN)	XP_011510033.1:p.Trp19151Ter
XM_017004819.1:c.83495G>A (TTN)	XP_016860308.1:p.Trp27832Ter
XM_017004820.1:c.78893G>A (TTN)	XP_016860309.1:p.Trp26298Ter
XM_017004821.1:c.78890G>A (TTN)	XP_016860310.1:p.Trp26297Ter
XM_017004822.1:c.75932G>A (TTN)	XP_016860311.1:p.Trp25311Ter
XM_017004823.1:c.57548G>A (TTN)	XP_016860312.1:p.Trp19183Ter
XM_024453094.1:c.79043G>A (TTN)	XP_024308862.1:p.Trp26348Ter
XM_024453095.1:c.79040G>A (TTN)	XP_024308863.1:p.Trp26347Ter
XM_024453096.1:c.78473G>A (TTN)	XP_024308864.1:p.Trp26158Ter
XM_024453097.1:c.75815G>A (TTN)	XP_024308865.1:p.Trp25272Ter
XM_024453098.1:c.75734G>A (TTN)	XP_024308866.1:p.Trp25245Ter
XM_024453099.1:c.57497G>A (TTN)	XP_024308867.1:p.Trp19166Ter
XM_024453100.1:c.47351G>A (TTN)	XP_024308868.1:p.Trp15784Ter