Canonical Allele Identifier: CA349458816

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178588790C>A , CM000664.2:g.178588790C>A	GRCh38
NC_000002.11:g.179453517C>A , CM000664.1:g.179453517C>A	GRCh37
NC_000002.10:g.179161763C>A	NCBI36
NG_011618.3:g.247013G>T , LRG_391:g.247013G>T
NG_051363.1:g.70964C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.62935G>T (TTN) MANE Select	NP_001254479.2:p.Glu20979Ter
ENST00000589042.5:c.62935G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu20979Ter
NM_001256850.1:c.58012G>T (TTN)	NP_001243779.1:p.Glu19338Ter
NM_003319.4:c.35740G>T (TTN)	NP_003310.4:p.Glu11914Ter
NM_133378.4:c.55231G>T (TTN)	NP_596869.4:p.Glu18411Ter
NM_133432.3:c.36115G>T (TTN)	NP_597676.3:p.Glu12039Ter
NM_133437.4:c.36316G>T (TTN)	NP_597681.4:p.Glu12106Ter
NR_038271.1:n.597-8806C>A (TTN-AS1)
NR_038272.1:n.3189-2349C>A (TTN-AS1)
ENST00000342175.10:c.36316G>T (TTN)	ENSP00000340554.6:p.Glu12106Ter
ENST00000342175.11:c.36316G>T (TTN)	ENSP00000340554.6:p.Glu12106Ter
ENST00000342992.10:c.55231G>T (TTN)	ENSP00000343764.6:p.Glu18411Ter
ENST00000342992.11:c.55231G>T (TTN)	ENSP00000343764.6:p.Glu18411Ter
ENST00000359218.10:c.36115G>T (TTN)	ENSP00000352154.5:p.Glu12039Ter
ENST00000359218.9:c.36115G>T (TTN)	ENSP00000352154.5:p.Glu12039Ter
ENST00000460472.6:c.35740G>T (TTN)	ENSP00000434586.1:p.Glu11914Ter
ENST00000591111.5:c.58012G>T (TTN)	ENSP00000465570.1:p.Glu19338Ter
ENST00000615779.4:c.58012G>T (TTN)	ENSP00000483597.1:p.Glu19338Ter
XM_011511729.1:c.62032G>T (TTN)	XP_011510031.1:p.Glu20678Ter
XM_011511730.1:c.35926G>T (TTN)	XP_011510032.1:p.Glu11976Ter
XM_011511731.1:c.35785G>T (TTN)	XP_011510033.1:p.Glu11929Ter
XM_017004819.1:c.61828G>T (TTN)	XP_016860308.1:p.Glu20610Ter
XM_017004820.1:c.57226G>T (TTN)	XP_016860309.1:p.Glu19076Ter
XM_017004821.1:c.57223G>T (TTN)	XP_016860310.1:p.Glu19075Ter
XM_017004822.1:c.54265G>T (TTN)	XP_016860311.1:p.Glu18089Ter
XM_017004823.1:c.35881G>T (TTN)	XP_016860312.1:p.Glu11961Ter
XM_024453094.1:c.57376G>T (TTN)	XP_024308862.1:p.Glu19126Ter
XM_024453095.1:c.57373G>T (TTN)	XP_024308863.1:p.Glu19125Ter
XM_024453096.1:c.56806G>T (TTN)	XP_024308864.1:p.Glu18936Ter
XM_024453097.1:c.54148G>T (TTN)	XP_024308865.1:p.Glu18050Ter
XM_024453098.1:c.54067G>T (TTN)	XP_024308866.1:p.Glu18023Ter
XM_024453099.1:c.35830G>T (TTN)	XP_024308867.1:p.Glu11944Ter
XM_024453100.1:c.25684G>T (TTN)	XP_024308868.1:p.Glu8562Ter