Canonical Allele Identifier: CA1310537103

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584628_178584629delinsTA , CM000664.2:g.178584628_178584629delinsTA	GRCh38
NC_000002.11:g.179449355_179449356delinsTA , CM000664.1:g.179449355_179449356delinsTA	GRCh37
NC_000002.10:g.179157601_179157602delinsTA	NCBI36
NG_011618.3:g.251174_251175delinsTA , LRG_391:g.251174_251175delinsTA
NG_051363.1:g.66802_66803delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.57268+40_57268+41delinsTA (TTN)	ENSP00000343764.6:n.57268+40_57268+41delinsTA
ENST00000342175.11:c.38353+40_38353+41delinsTA (TTN)	ENSP00000340554.6:n.38353+40_38353+41delinsTA
ENST00000359218.10:c.38152+40_38152+41delinsTA (TTN)	ENSP00000352154.5:n.38152+40_38152+41delinsTA
ENST00000342175.10:c.38353+40_38353+41delinsTA (TTN)	ENSP00000340554.6:n.38353+40_38353+41delinsTA
ENST00000342992.10:c.57268+40_57268+41delinsTA (TTN)	ENSP00000343764.6:n.57268+40_57268+41delinsTA
ENST00000359218.9:c.38152+40_38152+41delinsTA (TTN)	ENSP00000352154.5:n.38152+40_38152+41delinsTA
ENST00000460472.6:c.37777+40_37777+41delinsTA (TTN)	ENSP00000434586.1:n.37777+40_37777+41delinsTA
ENST00000589042.5:c.64972+40_64972+41delinsTA (TTN) MANE Select	ENSP00000467141.1:n.64972+40_64972+41delinsTA
ENST00000591111.5:c.60049+40_60049+41delinsTA (TTN)	ENSP00000465570.1:n.60049+40_60049+41delinsTA
ENST00000615779.4:c.60049+40_60049+41delinsTA (TTN)	ENSP00000483597.1:n.60049+40_60049+41delinsTA
NM_001256850.1:c.60049+40_60049+41delinsTA (TTN)	NP_001243779.1:n.60049+40_60049+41delinsTA
NM_001267550.2:c.64972+40_64972+41delinsTA (TTN) MANE Select	NP_001254479.2:n.64972+40_64972+41delinsTA
NM_003319.4:c.37777+40_37777+41delinsTA (TTN)	NP_003310.4:n.37777+40_37777+41delinsTA
NM_133378.4:c.57268+40_57268+41delinsTA (TTN)	NP_596869.4:n.57268+40_57268+41delinsTA
NM_133432.3:c.38152+40_38152+41delinsTA (TTN)	NP_597676.3:n.38152+40_38152+41delinsTA
NM_133437.4:c.38353+40_38353+41delinsTA (TTN)	NP_597681.4:n.38353+40_38353+41delinsTA
NR_038271.1:n.597-12968_597-12967delinsTA (TTN-AS1)
NR_038272.1:n.2823_2824delinsTA (TTN-AS1)
XM_011511729.1:c.64069+40_64069+41delinsTA (TTN)	XP_011510031.1:n.64069+40_64069+41delinsTA
XM_011511730.1:c.37963+40_37963+41delinsTA (TTN)	XP_011510032.1:n.37963+40_37963+41delinsTA
XM_011511731.1:c.37822+40_37822+41delinsTA (TTN)	XP_011510033.1:n.37822+40_37822+41delinsTA
XM_017004819.1:c.63865+40_63865+41delinsTA (TTN)	XP_016860308.1:n.63865+40_63865+41delinsTA
XM_017004820.1:c.59263+40_59263+41delinsTA (TTN)	XP_016860309.1:n.59263+40_59263+41delinsTA
XM_017004821.1:c.59260+40_59260+41delinsTA (TTN)	XP_016860310.1:n.59260+40_59260+41delinsTA
XM_017004822.1:c.56302+40_56302+41delinsTA (TTN)	XP_016860311.1:n.56302+40_56302+41delinsTA
XM_017004823.1:c.37918+40_37918+41delinsTA (TTN)	XP_016860312.1:n.37918+40_37918+41delinsTA
XM_024453094.1:c.59413+40_59413+41delinsTA (TTN)	XP_024308862.1:n.59413+40_59413+41delinsTA
XM_024453095.1:c.59410+40_59410+41delinsTA (TTN)	XP_024308863.1:n.59410+40_59410+41delinsTA
XM_024453096.1:c.58843+40_58843+41delinsTA (TTN)	XP_024308864.1:n.58843+40_58843+41delinsTA
XM_024453097.1:c.56185+40_56185+41delinsTA (TTN)	XP_024308865.1:n.56185+40_56185+41delinsTA
XM_024453098.1:c.56104+40_56104+41delinsTA (TTN)	XP_024308866.1:n.56104+40_56104+41delinsTA
XM_024453099.1:c.37867+40_37867+41delinsTA (TTN)	XP_024308867.1:n.37867+40_37867+41delinsTA
XM_024453100.1:c.27721+40_27721+41delinsTA (TTN)	XP_024308868.1:n.27721+40_27721+41delinsTA