Canonical Allele Identifier: CA1990539

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178573983T>C , CM000664.2:g.178573983T>C	GRCh38
NC_000002.11:g.179438710T>C , CM000664.1:g.179438710T>C	GRCh37
NC_000002.10:g.179146956T>C	NCBI36
NG_011618.3:g.261820A>G , LRG_391:g.261820A>G
NG_051363.1:g.56157T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.72149A>G (TTN) MANE Select	NP_001254479.2:p.Glu24050Gly
ENST00000589042.5:c.72149A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu24050Gly
NM_001256850.1:c.67226A>G (TTN)	NP_001243779.1:p.Glu22409Gly
NM_003319.4:c.44954A>G (TTN)	NP_003310.4:p.Glu14985Gly
NM_133378.4:c.64445A>G (TTN)	NP_596869.4:p.Glu21482Gly
NM_133432.3:c.45329A>G (TTN)	NP_597676.3:p.Glu15110Gly
NM_133437.4:c.45530A>G (TTN)	NP_597681.4:p.Glu15177Gly
NR_038271.1:n.596+2534T>C (TTN-AS1)
NR_038272.1:n.2044-8589T>C (TTN-AS1)
ENST00000342175.10:c.45530A>G (TTN)	ENSP00000340554.6:p.Glu15177Gly
ENST00000342175.11:c.45530A>G (TTN)	ENSP00000340554.6:p.Glu15177Gly
ENST00000342992.10:c.64445A>G (TTN)	ENSP00000343764.6:p.Glu21482Gly
ENST00000342992.11:c.64445A>G (TTN)	ENSP00000343764.6:p.Glu21482Gly
ENST00000359218.10:c.45329A>G (TTN)	ENSP00000352154.5:p.Glu15110Gly
ENST00000359218.9:c.45329A>G (TTN)	ENSP00000352154.5:p.Glu15110Gly
ENST00000460472.6:c.44954A>G (TTN)	ENSP00000434586.1:p.Glu14985Gly
ENST00000591111.5:c.67226A>G (TTN)	ENSP00000465570.1:p.Glu22409Gly
ENST00000615779.4:c.67226A>G (TTN)	ENSP00000483597.1:p.Glu22409Gly
XM_011511729.1:c.71246A>G (TTN)	XP_011510031.1:p.Glu23749Gly
XM_011511730.1:c.45140A>G (TTN)	XP_011510032.1:p.Glu15047Gly
XM_011511731.1:c.44999A>G (TTN)	XP_011510033.1:p.Glu15000Gly
XM_017004819.1:c.71042A>G (TTN)	XP_016860308.1:p.Glu23681Gly
XM_017004820.1:c.66440A>G (TTN)	XP_016860309.1:p.Glu22147Gly
XM_017004821.1:c.66437A>G (TTN)	XP_016860310.1:p.Glu22146Gly
XM_017004822.1:c.63479A>G (TTN)	XP_016860311.1:p.Glu21160Gly
XM_017004823.1:c.45095A>G (TTN)	XP_016860312.1:p.Glu15032Gly
XM_024453094.1:c.66590A>G (TTN)	XP_024308862.1:p.Glu22197Gly
XM_024453095.1:c.66587A>G (TTN)	XP_024308863.1:p.Glu22196Gly
XM_024453096.1:c.66020A>G (TTN)	XP_024308864.1:p.Glu22007Gly
XM_024453097.1:c.63362A>G (TTN)	XP_024308865.1:p.Glu21121Gly
XM_024453098.1:c.63281A>G (TTN)	XP_024308866.1:p.Glu21094Gly
XM_024453099.1:c.45044A>G (TTN)	XP_024308867.1:p.Glu15015Gly
XM_024453100.1:c.34898A>G (TTN)	XP_024308868.1:p.Glu11633Gly