Canonical Allele Identifier: CA1989764

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568639C>T , CM000664.2:g.178568639C>T	GRCh38
NC_000002.11:g.179433366C>T , CM000664.1:g.179433366C>T	GRCh37
NC_000002.10:g.179141612C>T	NCBI36
NG_011618.3:g.267164G>A , LRG_391:g.267164G>A
NG_051363.1:g.50813C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.77493G>A (TTN) MANE Select	NP_001254479.2:p.Trp25831Ter
ENST00000589042.5:c.77493G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp25831Ter
NM_001256850.1:c.72570G>A (TTN)	NP_001243779.1:p.Trp24190Ter
NM_003319.4:c.50298G>A (TTN)	NP_003310.4:p.Trp16766Ter
NM_133378.4:c.69789G>A (TTN)	NP_596869.4:p.Trp23263Ter
NM_133432.3:c.50673G>A (TTN)	NP_597676.3:p.Trp16891Ter
NM_133437.4:c.50874G>A (TTN)	NP_597681.4:p.Trp16958Ter
NR_038271.1:n.447-2661C>T (TTN-AS1)
NR_038272.1:n.2044-13933C>T (TTN-AS1)
ENST00000342175.10:c.50874G>A (TTN)	ENSP00000340554.6:p.Trp16958Ter
ENST00000342175.11:c.50874G>A (TTN)	ENSP00000340554.6:p.Trp16958Ter
ENST00000342992.10:c.69789G>A (TTN)	ENSP00000343764.6:p.Trp23263Ter
ENST00000342992.11:c.69789G>A (TTN)	ENSP00000343764.6:p.Trp23263Ter
ENST00000359218.10:c.50673G>A (TTN)	ENSP00000352154.5:p.Trp16891Ter
ENST00000359218.9:c.50673G>A (TTN)	ENSP00000352154.5:p.Trp16891Ter
ENST00000460472.6:c.50298G>A (TTN)	ENSP00000434586.1:p.Trp16766Ter
ENST00000591111.5:c.72570G>A (TTN)	ENSP00000465570.1:p.Trp24190Ter
ENST00000615779.4:c.72570G>A (TTN)	ENSP00000483597.1:p.Trp24190Ter
XM_011511729.1:c.76590G>A (TTN)	XP_011510031.1:p.Trp25530Ter
XM_011511730.1:c.50484G>A (TTN)	XP_011510032.1:p.Trp16828Ter
XM_011511731.1:c.50343G>A (TTN)	XP_011510033.1:p.Trp16781Ter
XM_017004819.1:c.76386G>A (TTN)	XP_016860308.1:p.Trp25462Ter
XM_017004820.1:c.71784G>A (TTN)	XP_016860309.1:p.Trp23928Ter
XM_017004821.1:c.71781G>A (TTN)	XP_016860310.1:p.Trp23927Ter
XM_017004822.1:c.68823G>A (TTN)	XP_016860311.1:p.Trp22941Ter
XM_017004823.1:c.50439G>A (TTN)	XP_016860312.1:p.Trp16813Ter
XM_024453094.1:c.71934G>A (TTN)	XP_024308862.1:p.Trp23978Ter
XM_024453095.1:c.71931G>A (TTN)	XP_024308863.1:p.Trp23977Ter
XM_024453096.1:c.71364G>A (TTN)	XP_024308864.1:p.Trp23788Ter
XM_024453097.1:c.68706G>A (TTN)	XP_024308865.1:p.Trp22902Ter
XM_024453098.1:c.68625G>A (TTN)	XP_024308866.1:p.Trp22875Ter
XM_024453099.1:c.50388G>A (TTN)	XP_024308867.1:p.Trp16796Ter
XM_024453100.1:c.40242G>A (TTN)	XP_024308868.1:p.Trp13414Ter