Canonical Allele Identifier: CA1310537114

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178584658_178584659delinsCA , CM000664.2:g.178584658_178584659delinsCA	GRCh38
NC_000002.11:g.179449385_179449386delinsCA , CM000664.1:g.179449385_179449386delinsCA	GRCh37
NC_000002.10:g.179157631_179157632delinsCA	NCBI36
NG_011618.3:g.251144_251145delinsTG , LRG_391:g.251144_251145delinsTG
NG_051363.1:g.66832_66833delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.57268+10_57268+11delinsTG (TTN)	ENSP00000343764.6:n.57268+10_57268+11delinsTG
ENST00000342175.11:c.38353+10_38353+11delinsTG (TTN)	ENSP00000340554.6:n.38353+10_38353+11delinsTG
ENST00000359218.10:c.38152+10_38152+11delinsTG (TTN)	ENSP00000352154.5:n.38152+10_38152+11delinsTG
ENST00000342175.10:c.38353+10_38353+11delinsTG (TTN)	ENSP00000340554.6:n.38353+10_38353+11delinsTG
ENST00000342992.10:c.57268+10_57268+11delinsTG (TTN)	ENSP00000343764.6:n.57268+10_57268+11delinsTG
ENST00000359218.9:c.38152+10_38152+11delinsTG (TTN)	ENSP00000352154.5:n.38152+10_38152+11delinsTG
ENST00000460472.6:c.37777+10_37777+11delinsTG (TTN)	ENSP00000434586.1:n.37777+10_37777+11delinsTG
ENST00000589042.5:c.64972+10_64972+11delinsTG (TTN) MANE Select	ENSP00000467141.1:n.64972+10_64972+11delinsTG
ENST00000591111.5:c.60049+10_60049+11delinsTG (TTN)	ENSP00000465570.1:n.60049+10_60049+11delinsTG
ENST00000615779.4:c.60049+10_60049+11delinsTG (TTN)	ENSP00000483597.1:n.60049+10_60049+11delinsTG
NM_001256850.1:c.60049+10_60049+11delinsTG (TTN)	NP_001243779.1:n.60049+10_60049+11delinsTG
NM_001267550.2:c.64972+10_64972+11delinsTG (TTN) MANE Select	NP_001254479.2:n.64972+10_64972+11delinsTG
NM_003319.4:c.37777+10_37777+11delinsTG (TTN)	NP_003310.4:n.37777+10_37777+11delinsTG
NM_133378.4:c.57268+10_57268+11delinsTG (TTN)	NP_596869.4:n.57268+10_57268+11delinsTG
NM_133432.3:c.38152+10_38152+11delinsTG (TTN)	NP_597676.3:n.38152+10_38152+11delinsTG
NM_133437.4:c.38353+10_38353+11delinsTG (TTN)	NP_597681.4:n.38353+10_38353+11delinsTG
NR_038271.1:n.597-12938_597-12937delinsCA (TTN-AS1)
NR_038272.1:n.2853_2854delinsCA (TTN-AS1)
XM_011511729.1:c.64069+10_64069+11delinsTG (TTN)	XP_011510031.1:n.64069+10_64069+11delinsTG
XM_011511730.1:c.37963+10_37963+11delinsTG (TTN)	XP_011510032.1:n.37963+10_37963+11delinsTG
XM_011511731.1:c.37822+10_37822+11delinsTG (TTN)	XP_011510033.1:n.37822+10_37822+11delinsTG
XM_017004819.1:c.63865+10_63865+11delinsTG (TTN)	XP_016860308.1:n.63865+10_63865+11delinsTG
XM_017004820.1:c.59263+10_59263+11delinsTG (TTN)	XP_016860309.1:n.59263+10_59263+11delinsTG
XM_017004821.1:c.59260+10_59260+11delinsTG (TTN)	XP_016860310.1:n.59260+10_59260+11delinsTG
XM_017004822.1:c.56302+10_56302+11delinsTG (TTN)	XP_016860311.1:n.56302+10_56302+11delinsTG
XM_017004823.1:c.37918+10_37918+11delinsTG (TTN)	XP_016860312.1:n.37918+10_37918+11delinsTG
XM_024453094.1:c.59413+10_59413+11delinsTG (TTN)	XP_024308862.1:n.59413+10_59413+11delinsTG
XM_024453095.1:c.59410+10_59410+11delinsTG (TTN)	XP_024308863.1:n.59410+10_59410+11delinsTG
XM_024453096.1:c.58843+10_58843+11delinsTG (TTN)	XP_024308864.1:n.58843+10_58843+11delinsTG
XM_024453097.1:c.56185+10_56185+11delinsTG (TTN)	XP_024308865.1:n.56185+10_56185+11delinsTG
XM_024453098.1:c.56104+10_56104+11delinsTG (TTN)	XP_024308866.1:n.56104+10_56104+11delinsTG
XM_024453099.1:c.37867+10_37867+11delinsTG (TTN)	XP_024308867.1:n.37867+10_37867+11delinsTG
XM_024453100.1:c.27721+10_27721+11delinsTG (TTN)	XP_024308868.1:n.27721+10_27721+11delinsTG