Canonical Allele Identifier: CA349588691

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178565674G>A , CM000664.2:g.178565674G>A	GRCh38
NC_000002.11:g.179430401G>A , CM000664.1:g.179430401G>A	GRCh37
NC_000002.10:g.179138647G>A	NCBI36
NG_011618.3:g.270129C>T , LRG_391:g.270129C>T
NG_051363.1:g.47848G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.80458C>T (TTN) MANE Select	NP_001254479.2:p.Gln26820Ter
ENST00000589042.5:c.80458C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln26820Ter
NM_001256850.1:c.75535C>T (TTN)	NP_001243779.1:p.Gln25179Ter
NM_003319.4:c.53263C>T (TTN)	NP_003310.4:p.Gln17755Ter
NM_133378.4:c.72754C>T (TTN)	NP_596869.4:p.Gln24252Ter
NM_133432.3:c.53638C>T (TTN)	NP_597676.3:p.Gln17880Ter
NM_133437.4:c.53839C>T (TTN)	NP_597681.4:p.Gln17947Ter
NR_038271.1:n.447-5626G>A (TTN-AS1)
NR_038272.1:n.2044-16898G>A (TTN-AS1)
ENST00000342175.10:c.53839C>T (TTN)	ENSP00000340554.6:p.Gln17947Ter
ENST00000342175.11:c.53839C>T (TTN)	ENSP00000340554.6:p.Gln17947Ter
ENST00000342992.10:c.72754C>T (TTN)	ENSP00000343764.6:p.Gln24252Ter
ENST00000342992.11:c.72754C>T (TTN)	ENSP00000343764.6:p.Gln24252Ter
ENST00000359218.10:c.53638C>T (TTN)	ENSP00000352154.5:p.Gln17880Ter
ENST00000359218.9:c.53638C>T (TTN)	ENSP00000352154.5:p.Gln17880Ter
ENST00000460472.6:c.53263C>T (TTN)	ENSP00000434586.1:p.Gln17755Ter
ENST00000591111.5:c.75535C>T (TTN)	ENSP00000465570.1:p.Gln25179Ter
ENST00000615779.4:c.75535C>T (TTN)	ENSP00000483597.1:p.Gln25179Ter
XM_011511729.1:c.79555C>T (TTN)	XP_011510031.1:p.Gln26519Ter
XM_011511730.1:c.53449C>T (TTN)	XP_011510032.1:p.Gln17817Ter
XM_011511731.1:c.53308C>T (TTN)	XP_011510033.1:p.Gln17770Ter
XM_017004819.1:c.79351C>T (TTN)	XP_016860308.1:p.Gln26451Ter
XM_017004820.1:c.74749C>T (TTN)	XP_016860309.1:p.Gln24917Ter
XM_017004821.1:c.74746C>T (TTN)	XP_016860310.1:p.Gln24916Ter
XM_017004822.1:c.71788C>T (TTN)	XP_016860311.1:p.Gln23930Ter
XM_017004823.1:c.53404C>T (TTN)	XP_016860312.1:p.Gln17802Ter
XM_024453094.1:c.74899C>T (TTN)	XP_024308862.1:p.Gln24967Ter
XM_024453095.1:c.74896C>T (TTN)	XP_024308863.1:p.Gln24966Ter
XM_024453096.1:c.74329C>T (TTN)	XP_024308864.1:p.Gln24777Ter
XM_024453097.1:c.71671C>T (TTN)	XP_024308865.1:p.Gln23891Ter
XM_024453098.1:c.71590C>T (TTN)	XP_024308866.1:p.Gln23864Ter
XM_024453099.1:c.53353C>T (TTN)	XP_024308867.1:p.Gln17785Ter
XM_024453100.1:c.43207C>T (TTN)	XP_024308868.1:p.Gln14403Ter