Canonical Allele Identifier: CA1989102

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178563891C>T , CM000664.2:g.178563891C>T	GRCh38
NC_000002.11:g.179428618C>T , CM000664.1:g.179428618C>T	GRCh37
NC_000002.10:g.179136864C>T	NCBI36
NG_011618.3:g.271912G>A , LRG_391:g.271912G>A
NG_051363.1:g.46065C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.82241G>A (TTN) MANE Select	NP_001254479.2:p.Arg27414Gln
ENST00000589042.5:c.82241G>A (TTN) MANE Select	ENSP00000467141.1:p.Arg27414Gln
NM_001256850.1:c.77318G>A (TTN)	NP_001243779.1:p.Arg25773Gln
NM_003319.4:c.55046G>A (TTN)	NP_003310.4:p.Arg18349Gln
NM_133378.4:c.74537G>A (TTN)	NP_596869.4:p.Arg24846Gln
NM_133432.3:c.55421G>A (TTN)	NP_597676.3:p.Arg18474Gln
NM_133437.4:c.55622G>A (TTN)	NP_597681.4:p.Arg18541Gln
NR_038271.1:n.447-7409C>T (TTN-AS1)
NR_038272.1:n.2044-18681C>T (TTN-AS1)
ENST00000342175.10:c.55622G>A (TTN)	ENSP00000340554.6:p.Arg18541Gln
ENST00000342175.11:c.55622G>A (TTN)	ENSP00000340554.6:p.Arg18541Gln
ENST00000342992.10:c.74537G>A (TTN)	ENSP00000343764.6:p.Arg24846Gln
ENST00000342992.11:c.74537G>A (TTN)	ENSP00000343764.6:p.Arg24846Gln
ENST00000359218.10:c.55421G>A (TTN)	ENSP00000352154.5:p.Arg18474Gln
ENST00000359218.9:c.55421G>A (TTN)	ENSP00000352154.5:p.Arg18474Gln
ENST00000460472.6:c.55046G>A (TTN)	ENSP00000434586.1:p.Arg18349Gln
ENST00000591111.5:c.77318G>A (TTN)	ENSP00000465570.1:p.Arg25773Gln
ENST00000615779.4:c.77318G>A (TTN)	ENSP00000483597.1:p.Arg25773Gln
XM_011511729.1:c.81338G>A (TTN)	XP_011510031.1:p.Arg27113Gln
XM_011511730.1:c.55232G>A (TTN)	XP_011510032.1:p.Arg18411Gln
XM_011511731.1:c.55091G>A (TTN)	XP_011510033.1:p.Arg18364Gln
XM_017004819.1:c.81134G>A (TTN)	XP_016860308.1:p.Arg27045Gln
XM_017004820.1:c.76532G>A (TTN)	XP_016860309.1:p.Arg25511Gln
XM_017004821.1:c.76529G>A (TTN)	XP_016860310.1:p.Arg25510Gln
XM_017004822.1:c.73571G>A (TTN)	XP_016860311.1:p.Arg24524Gln
XM_017004823.1:c.55187G>A (TTN)	XP_016860312.1:p.Arg18396Gln
XM_024453094.1:c.76682G>A (TTN)	XP_024308862.1:p.Arg25561Gln
XM_024453095.1:c.76679G>A (TTN)	XP_024308863.1:p.Arg25560Gln
XM_024453096.1:c.76112G>A (TTN)	XP_024308864.1:p.Arg25371Gln
XM_024453097.1:c.73454G>A (TTN)	XP_024308865.1:p.Arg24485Gln
XM_024453098.1:c.73373G>A (TTN)	XP_024308866.1:p.Arg24458Gln
XM_024453099.1:c.55136G>A (TTN)	XP_024308867.1:p.Arg18379Gln
XM_024453100.1:c.44990G>A (TTN)	XP_024308868.1:p.Arg14997Gln