Canonical Allele Identifier: CA1994793

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178615400T>G , CM000664.2:g.178615400T>G	GRCh38
NC_000002.11:g.179480127T>G , CM000664.1:g.179480127T>G	GRCh37
NC_000002.10:g.179188372T>G	NCBI36
NG_011618.3:g.220403A>C , LRG_391:g.220403A>C
NG_051363.1:g.97574T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.40841A>C (TTN)	ENSP00000343764.6:p.Asp13614Ala
ENST00000342175.11:c.21926A>C (TTN)	ENSP00000340554.6:p.Asp7309Ala
ENST00000359218.10:c.21725A>C (TTN)	ENSP00000352154.5:p.Asp7242Ala
ENST00000342175.10:c.21926A>C (TTN)	ENSP00000340554.6:p.Asp7309Ala
ENST00000342992.10:c.40841A>C (TTN)	ENSP00000343764.6:p.Asp13614Ala
ENST00000359218.9:c.21725A>C (TTN)	ENSP00000352154.5:p.Asp7242Ala
ENST00000460472.6:c.21350A>C (TTN)	ENSP00000434586.1:p.Asp7117Ala
ENST00000589042.5:c.48545A>C (TTN) MANE Select	ENSP00000467141.1:p.Asp16182Ala
ENST00000591111.5:c.43622A>C (TTN)	ENSP00000465570.1:p.Asp14541Ala
ENST00000615779.4:c.43622A>C (TTN)	ENSP00000483597.1:p.Asp14541Ala
NM_001256850.1:c.43622A>C (TTN)	NP_001243779.1:p.Asp14541Ala
NM_001267550.2:c.48545A>C (TTN) MANE Select	NP_001254479.2:p.Asp16182Ala
NM_003319.4:c.21350A>C (TTN)	NP_003310.4:p.Asp7117Ala
NM_133378.4:c.40841A>C (TTN)	NP_596869.4:p.Asp13614Ala
NM_133432.3:c.21725A>C (TTN)	NP_597676.3:p.Asp7242Ala
NM_133437.4:c.21926A>C (TTN)	NP_597681.4:p.Asp7309Ala
NR_038271.1:n.1604+26T>G (TTN-AS1)
XM_011511729.1:c.47642A>C (TTN)	XP_011510031.1:p.Asp15881Ala
XM_011511730.1:c.21536A>C (TTN)	XP_011510032.1:p.Asp7179Ala
XM_011511731.1:c.21395A>C (TTN)	XP_011510033.1:p.Asp7132Ala
XM_017004819.1:c.47438A>C (TTN)	XP_016860308.1:p.Asp15813Ala
XM_017004820.1:c.42836A>C (TTN)	XP_016860309.1:p.Asp14279Ala
XM_017004821.1:c.42833A>C (TTN)	XP_016860310.1:p.Asp14278Ala
XM_017004822.1:c.39875A>C (TTN)	XP_016860311.1:p.Asp13292Ala
XM_017004823.1:c.21491A>C (TTN)	XP_016860312.1:p.Asp7164Ala
XM_024453094.1:c.42986A>C (TTN)	XP_024308862.1:p.Asp14329Ala
XM_024453095.1:c.42983A>C (TTN)	XP_024308863.1:p.Asp14328Ala
XM_024453096.1:c.42416A>C (TTN)	XP_024308864.1:p.Asp14139Ala
XM_024453097.1:c.39758A>C (TTN)	XP_024308865.1:p.Asp13253Ala
XM_024453098.1:c.39677A>C (TTN)	XP_024308866.1:p.Asp13226Ala
XM_024453099.1:c.21440A>C (TTN)	XP_024308867.1:p.Asp7147Ala
XM_024453100.1:c.11294A>C (TTN)	XP_024308868.1:p.Asp3765Ala