Canonical Allele Identifier: CA349591689

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178611371C>T , CM000664.2:g.178611371C>T	GRCh38
NC_000002.11:g.179476098C>T , CM000664.1:g.179476098C>T	GRCh37
NC_000002.10:g.179184343C>T	NCBI36
NG_011618.3:g.224432G>A , LRG_391:g.224432G>A
NG_051363.1:g.93545C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.50857+1G>A (TTN) MANE Select	NP_001254479.2:n.50857+1G>A
ENST00000589042.5:c.50857+1G>A (TTN) MANE Select	ENSP00000467141.1:n.50857+1G>A
NM_001256850.1:c.45934+1G>A (TTN)	NP_001243779.1:n.45934+1G>A
NM_003319.4:c.23662+1G>A (TTN)	NP_003310.4:n.23662+1G>A
NM_133378.4:c.43153+1G>A (TTN)	NP_596869.4:n.43153+1G>A
NM_133432.3:c.24037+1G>A (TTN)	NP_597676.3:n.24037+1G>A
NM_133437.4:c.24238+1G>A (TTN)	NP_597681.4:n.24238+1G>A
NR_038271.1:n.783-2664C>T (TTN-AS1)
ENST00000342175.10:c.24238+1G>A (TTN)	ENSP00000340554.6:n.24238+1G>A
ENST00000342175.11:c.24238+1G>A (TTN)	ENSP00000340554.6:n.24238+1G>A
ENST00000342992.10:c.43153+1G>A (TTN)	ENSP00000343764.6:n.43153+1G>A
ENST00000342992.11:c.43153+1G>A (TTN)	ENSP00000343764.6:n.43153+1G>A
ENST00000359218.10:c.24037+1G>A (TTN)	ENSP00000352154.5:n.24037+1G>A
ENST00000359218.9:c.24037+1G>A (TTN)	ENSP00000352154.5:n.24037+1G>A
ENST00000460472.6:c.23662+1G>A (TTN)	ENSP00000434586.1:n.23662+1G>A
ENST00000591111.5:c.45934+1G>A (TTN)	ENSP00000465570.1:n.45934+1G>A
ENST00000615779.4:c.45934+1G>A (TTN)	ENSP00000483597.1:n.45934+1G>A
XM_011511729.1:c.49954+1G>A (TTN)	XP_011510031.1:n.49954+1G>A
XM_011511730.1:c.23848+1G>A (TTN)	XP_011510032.1:n.23848+1G>A
XM_011511731.1:c.23707+1G>A (TTN)	XP_011510033.1:n.23707+1G>A
XM_017004819.1:c.49750+1G>A (TTN)	XP_016860308.1:n.49750+1G>A
XM_017004820.1:c.45148+1G>A (TTN)	XP_016860309.1:n.45148+1G>A
XM_017004821.1:c.45145+1G>A (TTN)	XP_016860310.1:n.45145+1G>A
XM_017004822.1:c.42187+1G>A (TTN)	XP_016860311.1:n.42187+1G>A
XM_017004823.1:c.23803+1G>A (TTN)	XP_016860312.1:n.23803+1G>A
XM_024453094.1:c.45298+1G>A (TTN)	XP_024308862.1:n.45298+1G>A
XM_024453095.1:c.45295+1G>A (TTN)	XP_024308863.1:n.45295+1G>A
XM_024453096.1:c.44728+1G>A (TTN)	XP_024308864.1:n.44728+1G>A
XM_024453097.1:c.42070+1G>A (TTN)	XP_024308865.1:n.42070+1G>A
XM_024453098.1:c.41989+1G>A (TTN)	XP_024308866.1:n.41989+1G>A
XM_024453099.1:c.23752+1G>A (TTN)	XP_024308867.1:n.23752+1G>A
XM_024453100.1:c.13606+1G>A (TTN)	XP_024308868.1:n.13606+1G>A