Canonical Allele Identifier: CA349589096

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178565752G>A , CM000664.2:g.178565752G>A	GRCh38
NC_000002.11:g.179430479G>A , CM000664.1:g.179430479G>A	GRCh37
NC_000002.10:g.179138725G>A	NCBI36
NG_011618.3:g.270051C>T , LRG_391:g.270051C>T
NG_051363.1:g.47926G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.80380C>T (TTN) MANE Select	NP_001254479.2:p.Gln26794Ter
ENST00000589042.5:c.80380C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln26794Ter
NM_001256850.1:c.75457C>T (TTN)	NP_001243779.1:p.Gln25153Ter
NM_003319.4:c.53185C>T (TTN)	NP_003310.4:p.Gln17729Ter
NM_133378.4:c.72676C>T (TTN)	NP_596869.4:p.Gln24226Ter
NM_133432.3:c.53560C>T (TTN)	NP_597676.3:p.Gln17854Ter
NM_133437.4:c.53761C>T (TTN)	NP_597681.4:p.Gln17921Ter
NR_038271.1:n.447-5548G>A (TTN-AS1)
NR_038272.1:n.2044-16820G>A (TTN-AS1)
ENST00000342175.10:c.53761C>T (TTN)	ENSP00000340554.6:p.Gln17921Ter
ENST00000342175.11:c.53761C>T (TTN)	ENSP00000340554.6:p.Gln17921Ter
ENST00000342992.10:c.72676C>T (TTN)	ENSP00000343764.6:p.Gln24226Ter
ENST00000342992.11:c.72676C>T (TTN)	ENSP00000343764.6:p.Gln24226Ter
ENST00000359218.10:c.53560C>T (TTN)	ENSP00000352154.5:p.Gln17854Ter
ENST00000359218.9:c.53560C>T (TTN)	ENSP00000352154.5:p.Gln17854Ter
ENST00000460472.6:c.53185C>T (TTN)	ENSP00000434586.1:p.Gln17729Ter
ENST00000591111.5:c.75457C>T (TTN)	ENSP00000465570.1:p.Gln25153Ter
ENST00000615779.4:c.75457C>T (TTN)	ENSP00000483597.1:p.Gln25153Ter
XM_011511729.1:c.79477C>T (TTN)	XP_011510031.1:p.Gln26493Ter
XM_011511730.1:c.53371C>T (TTN)	XP_011510032.1:p.Gln17791Ter
XM_011511731.1:c.53230C>T (TTN)	XP_011510033.1:p.Gln17744Ter
XM_017004819.1:c.79273C>T (TTN)	XP_016860308.1:p.Gln26425Ter
XM_017004820.1:c.74671C>T (TTN)	XP_016860309.1:p.Gln24891Ter
XM_017004821.1:c.74668C>T (TTN)	XP_016860310.1:p.Gln24890Ter
XM_017004822.1:c.71710C>T (TTN)	XP_016860311.1:p.Gln23904Ter
XM_017004823.1:c.53326C>T (TTN)	XP_016860312.1:p.Gln17776Ter
XM_024453094.1:c.74821C>T (TTN)	XP_024308862.1:p.Gln24941Ter
XM_024453095.1:c.74818C>T (TTN)	XP_024308863.1:p.Gln24940Ter
XM_024453096.1:c.74251C>T (TTN)	XP_024308864.1:p.Gln24751Ter
XM_024453097.1:c.71593C>T (TTN)	XP_024308865.1:p.Gln23865Ter
XM_024453098.1:c.71512C>T (TTN)	XP_024308866.1:p.Gln23838Ter
XM_024453099.1:c.53275C>T (TTN)	XP_024308867.1:p.Gln17759Ter
XM_024453100.1:c.43129C>T (TTN)	XP_024308868.1:p.Gln14377Ter