Canonical Allele Identifier: CA349423953

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178579939G>A , CM000664.2:g.178579939G>A	GRCh38
NC_000002.11:g.179444666G>A , CM000664.1:g.179444666G>A	GRCh37
NC_000002.10:g.179152912G>A	NCBI36
NG_011618.3:g.255864C>T , LRG_391:g.255864C>T
NG_051363.1:g.62113G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.67348C>T (TTN) MANE Select	NP_001254479.2:p.Gln22450Ter
ENST00000589042.5:c.67348C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln22450Ter
NM_001256850.1:c.62425C>T (TTN)	NP_001243779.1:p.Gln20809Ter
NM_003319.4:c.40153C>T (TTN)	NP_003310.4:p.Gln13385Ter
NM_133378.4:c.59644C>T (TTN)	NP_596869.4:p.Gln19882Ter
NM_133432.3:c.40528C>T (TTN)	NP_597676.3:p.Gln13510Ter
NM_133437.4:c.40729C>T (TTN)	NP_597681.4:p.Gln13577Ter
NR_038271.1:n.596+8490G>A (TTN-AS1)
NR_038272.1:n.2044-2633G>A (TTN-AS1)
ENST00000342175.10:c.40729C>T (TTN)	ENSP00000340554.6:p.Gln13577Ter
ENST00000342175.11:c.40729C>T (TTN)	ENSP00000340554.6:p.Gln13577Ter
ENST00000342992.10:c.59644C>T (TTN)	ENSP00000343764.6:p.Gln19882Ter
ENST00000342992.11:c.59644C>T (TTN)	ENSP00000343764.6:p.Gln19882Ter
ENST00000359218.10:c.40528C>T (TTN)	ENSP00000352154.5:p.Gln13510Ter
ENST00000359218.9:c.40528C>T (TTN)	ENSP00000352154.5:p.Gln13510Ter
ENST00000460472.6:c.40153C>T (TTN)	ENSP00000434586.1:p.Gln13385Ter
ENST00000591111.5:c.62425C>T (TTN)	ENSP00000465570.1:p.Gln20809Ter
ENST00000615779.4:c.62425C>T (TTN)	ENSP00000483597.1:p.Gln20809Ter
XM_011511729.1:c.66445C>T (TTN)	XP_011510031.1:p.Gln22149Ter
XM_011511730.1:c.40339C>T (TTN)	XP_011510032.1:p.Gln13447Ter
XM_011511731.1:c.40198C>T (TTN)	XP_011510033.1:p.Gln13400Ter
XM_017004819.1:c.66241C>T (TTN)	XP_016860308.1:p.Gln22081Ter
XM_017004820.1:c.61639C>T (TTN)	XP_016860309.1:p.Gln20547Ter
XM_017004821.1:c.61636C>T (TTN)	XP_016860310.1:p.Gln20546Ter
XM_017004822.1:c.58678C>T (TTN)	XP_016860311.1:p.Gln19560Ter
XM_017004823.1:c.40294C>T (TTN)	XP_016860312.1:p.Gln13432Ter
XM_024453094.1:c.61789C>T (TTN)	XP_024308862.1:p.Gln20597Ter
XM_024453095.1:c.61786C>T (TTN)	XP_024308863.1:p.Gln20596Ter
XM_024453096.1:c.61219C>T (TTN)	XP_024308864.1:p.Gln20407Ter
XM_024453097.1:c.58561C>T (TTN)	XP_024308865.1:p.Gln19521Ter
XM_024453098.1:c.58480C>T (TTN)	XP_024308866.1:p.Gln19494Ter
XM_024453099.1:c.40243C>T (TTN)	XP_024308867.1:p.Gln13415Ter
XM_024453100.1:c.30097C>T (TTN)	XP_024308868.1:p.Gln10033Ter