Canonical Allele Identifier: CA349442432

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586656C>T , CM000664.2:g.178586656C>T	GRCh38
NC_000002.11:g.179451383C>T , CM000664.1:g.179451383C>T	GRCh37
NC_000002.10:g.179159629C>T	NCBI36
NG_011618.3:g.249147G>A , LRG_391:g.249147G>A
NG_051363.1:g.68830C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.64245G>A (TTN) MANE Select	NP_001254479.2:p.Trp21415Ter
ENST00000589042.5:c.64245G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp21415Ter
NM_001256850.1:c.59322G>A (TTN)	NP_001243779.1:p.Trp19774Ter
NM_003319.4:c.37050G>A (TTN)	NP_003310.4:p.Trp12350Ter
NM_133378.4:c.56541G>A (TTN)	NP_596869.4:p.Trp18847Ter
NM_133432.3:c.37425G>A (TTN)	NP_597676.3:p.Trp12475Ter
NM_133437.4:c.37626G>A (TTN)	NP_597681.4:p.Trp12542Ter
NR_038271.1:n.597-10940C>T (TTN-AS1)
NR_038272.1:n.3188+1663C>T (TTN-AS1)
ENST00000342175.10:c.37626G>A (TTN)	ENSP00000340554.6:p.Trp12542Ter
ENST00000342175.11:c.37626G>A (TTN)	ENSP00000340554.6:p.Trp12542Ter
ENST00000342992.10:c.56541G>A (TTN)	ENSP00000343764.6:p.Trp18847Ter
ENST00000342992.11:c.56541G>A (TTN)	ENSP00000343764.6:p.Trp18847Ter
ENST00000359218.10:c.37425G>A (TTN)	ENSP00000352154.5:p.Trp12475Ter
ENST00000359218.9:c.37425G>A (TTN)	ENSP00000352154.5:p.Trp12475Ter
ENST00000460472.6:c.37050G>A (TTN)	ENSP00000434586.1:p.Trp12350Ter
ENST00000591111.5:c.59322G>A (TTN)	ENSP00000465570.1:p.Trp19774Ter
ENST00000615779.4:c.59322G>A (TTN)	ENSP00000483597.1:p.Trp19774Ter
XM_011511729.1:c.63342G>A (TTN)	XP_011510031.1:p.Trp21114Ter
XM_011511730.1:c.37236G>A (TTN)	XP_011510032.1:p.Trp12412Ter
XM_011511731.1:c.37095G>A (TTN)	XP_011510033.1:p.Trp12365Ter
XM_017004819.1:c.63138G>A (TTN)	XP_016860308.1:p.Trp21046Ter
XM_017004820.1:c.58536G>A (TTN)	XP_016860309.1:p.Trp19512Ter
XM_017004821.1:c.58533G>A (TTN)	XP_016860310.1:p.Trp19511Ter
XM_017004822.1:c.55575G>A (TTN)	XP_016860311.1:p.Trp18525Ter
XM_017004823.1:c.37191G>A (TTN)	XP_016860312.1:p.Trp12397Ter
XM_024453094.1:c.58686G>A (TTN)	XP_024308862.1:p.Trp19562Ter
XM_024453095.1:c.58683G>A (TTN)	XP_024308863.1:p.Trp19561Ter
XM_024453096.1:c.58116G>A (TTN)	XP_024308864.1:p.Trp19372Ter
XM_024453097.1:c.55458G>A (TTN)	XP_024308865.1:p.Trp18486Ter
XM_024453098.1:c.55377G>A (TTN)	XP_024308866.1:p.Trp18459Ter
XM_024453099.1:c.37140G>A (TTN)	XP_024308867.1:p.Trp12380Ter
XM_024453100.1:c.26994G>A (TTN)	XP_024308868.1:p.Trp8998Ter