Canonical Allele Identifier: CA349424668

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178580321C>T , CM000664.2:g.178580321C>T	GRCh38
NC_000002.11:g.179445048C>T , CM000664.1:g.179445048C>T	GRCh37
NC_000002.10:g.179153294C>T	NCBI36
NG_011618.3:g.255482G>A , LRG_391:g.255482G>A
NG_051363.1:g.62495C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.67057+1G>A (TTN) MANE Select	NP_001254479.2:n.67057+1G>A
ENST00000589042.5:c.67057+1G>A (TTN) MANE Select	ENSP00000467141.1:n.67057+1G>A
NM_001256850.1:c.62134+1G>A (TTN)	NP_001243779.1:n.62134+1G>A
NM_003319.4:c.39862+1G>A (TTN)	NP_003310.4:n.39862+1G>A
NM_133378.4:c.59353+1G>A (TTN)	NP_596869.4:n.59353+1G>A
NM_133432.3:c.40237+1G>A (TTN)	NP_597676.3:n.40237+1G>A
NM_133437.4:c.40438+1G>A (TTN)	NP_597681.4:n.40438+1G>A
NR_038271.1:n.596+8872C>T (TTN-AS1)
NR_038272.1:n.2044-2251C>T (TTN-AS1)
ENST00000342175.10:c.40438+1G>A (TTN)	ENSP00000340554.6:n.40438+1G>A
ENST00000342175.11:c.40438+1G>A (TTN)	ENSP00000340554.6:n.40438+1G>A
ENST00000342992.10:c.59353+1G>A (TTN)	ENSP00000343764.6:n.59353+1G>A
ENST00000342992.11:c.59353+1G>A (TTN)	ENSP00000343764.6:n.59353+1G>A
ENST00000359218.10:c.40237+1G>A (TTN)	ENSP00000352154.5:n.40237+1G>A
ENST00000359218.9:c.40237+1G>A (TTN)	ENSP00000352154.5:n.40237+1G>A
ENST00000460472.6:c.39862+1G>A (TTN)	ENSP00000434586.1:n.39862+1G>A
ENST00000591111.5:c.62134+1G>A (TTN)	ENSP00000465570.1:n.62134+1G>A
ENST00000615779.4:c.62134+1G>A (TTN)	ENSP00000483597.1:n.62134+1G>A
XM_011511729.1:c.66154+1G>A (TTN)	XP_011510031.1:n.66154+1G>A
XM_011511730.1:c.40048+1G>A (TTN)	XP_011510032.1:n.40048+1G>A
XM_011511731.1:c.39907+1G>A (TTN)	XP_011510033.1:n.39907+1G>A
XM_017004819.1:c.65950+1G>A (TTN)	XP_016860308.1:n.65950+1G>A
XM_017004820.1:c.61348+1G>A (TTN)	XP_016860309.1:n.61348+1G>A
XM_017004821.1:c.61345+1G>A (TTN)	XP_016860310.1:n.61345+1G>A
XM_017004822.1:c.58387+1G>A (TTN)	XP_016860311.1:n.58387+1G>A
XM_017004823.1:c.40003+1G>A (TTN)	XP_016860312.1:n.40003+1G>A
XM_024453094.1:c.61498+1G>A (TTN)	XP_024308862.1:n.61498+1G>A
XM_024453095.1:c.61495+1G>A (TTN)	XP_024308863.1:n.61495+1G>A
XM_024453096.1:c.60928+1G>A (TTN)	XP_024308864.1:n.60928+1G>A
XM_024453097.1:c.58270+1G>A (TTN)	XP_024308865.1:n.58270+1G>A
XM_024453098.1:c.58189+1G>A (TTN)	XP_024308866.1:n.58189+1G>A
XM_024453099.1:c.39952+1G>A (TTN)	XP_024308867.1:n.39952+1G>A
XM_024453100.1:c.29806+1G>A (TTN)	XP_024308868.1:n.29806+1G>A