Canonical Allele Identifier: CA16604011

Gene: TTN TTN-AS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178607930G>T , CM000664.2:g.178607930G>T	GRCh38
NC_000002.11:g.179472657G>T , CM000664.1:g.179472657G>T	GRCh37
NC_000002.10:g.179180902G>T	NCBI36
NG_011618.3:g.227873C>A , LRG_391:g.227873C>A
NG_051363.1:g.90104G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.45153C>A (TTN)	ENSP00000343764.6:p.Cys15051Ter
ENST00000342175.11:c.26238C>A (TTN)	ENSP00000340554.6:p.Cys8746Ter
ENST00000359218.10:c.26037C>A (TTN)	ENSP00000352154.5:p.Cys8679Ter
ENST00000342175.10:c.26238C>A (TTN)	ENSP00000340554.6:p.Cys8746Ter
ENST00000342992.10:c.45153C>A (TTN)	ENSP00000343764.6:p.Cys15051Ter
ENST00000359218.9:c.26037C>A (TTN)	ENSP00000352154.5:p.Cys8679Ter
ENST00000460472.6:c.25662C>A (TTN)	ENSP00000434586.1:p.Cys8554Ter
ENST00000589042.5:c.52857C>A (TTN) MANE Select	ENSP00000467141.1:p.Cys17619Ter
ENST00000591111.5:c.47934C>A (TTN)	ENSP00000465570.1:p.Cys15978Ter
ENST00000615779.4:c.47934C>A (TTN)	ENSP00000483597.1:p.Cys15978Ter
NM_001256850.1:c.47934C>A (TTN)	NP_001243779.1:p.Cys15978Ter
NM_001267550.2:c.52857C>A (TTN) MANE Select	NP_001254479.2:p.Cys17619Ter
NM_003319.4:c.25662C>A (TTN)	NP_003310.4:p.Cys8554Ter
NM_133378.4:c.45153C>A (TTN)	NP_596869.4:p.Cys15051Ter
NM_133432.3:c.26037C>A (TTN)	NP_597676.3:p.Cys8679Ter
NM_133437.4:c.26238C>A (TTN)	NP_597681.4:p.Cys8746Ter
NR_038271.1:n.683-237G>T (TTN-AS1)
XM_011511729.1:c.51954C>A (TTN)	XP_011510031.1:p.Cys17318Ter
XM_011511730.1:c.25848C>A (TTN)	XP_011510032.1:p.Cys8616Ter
XM_011511731.1:c.25707C>A (TTN)	XP_011510033.1:p.Cys8569Ter
XM_017004819.1:c.51750C>A (TTN)	XP_016860308.1:p.Cys17250Ter
XM_017004820.1:c.47148C>A (TTN)	XP_016860309.1:p.Cys15716Ter
XM_017004821.1:c.47145C>A (TTN)	XP_016860310.1:p.Cys15715Ter
XM_017004822.1:c.44187C>A (TTN)	XP_016860311.1:p.Cys14729Ter
XM_017004823.1:c.25803C>A (TTN)	XP_016860312.1:p.Cys8601Ter
XM_024453094.1:c.47298C>A (TTN)	XP_024308862.1:p.Cys15766Ter
XM_024453095.1:c.47295C>A (TTN)	XP_024308863.1:p.Cys15765Ter
XM_024453096.1:c.46728C>A (TTN)	XP_024308864.1:p.Cys15576Ter
XM_024453097.1:c.44070C>A (TTN)	XP_024308865.1:p.Cys14690Ter
XM_024453098.1:c.43989C>A (TTN)	XP_024308866.1:p.Cys14663Ter
XM_024453099.1:c.25752C>A (TTN)	XP_024308867.1:p.Cys8584Ter
XM_024453100.1:c.15606C>A (TTN)	XP_024308868.1:p.Cys5202Ter