Canonical Allele Identifier: CA2567775021

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591932_178591933insC , CM000664.2:g.178591932_178591933insC	GRCh38
NC_000002.11:g.179456659_179456660insC , CM000664.1:g.179456659_179456660insC	GRCh37
NC_000002.10:g.179164905_179164906insC	NCBI36
NG_011618.3:g.243870_243871insG , LRG_391:g.243870_243871insG
NG_051363.1:g.74106_74107insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52223-41_52223-40insG (TTN)	ENSP00000343764.6:n.52223-41_52223-40insG
ENST00000342175.11:c.33308-41_33308-40insG (TTN)	ENSP00000340554.6:n.33308-41_33308-40insG
ENST00000359218.10:c.33107-41_33107-40insG (TTN)	ENSP00000352154.5:n.33107-41_33107-40insG
ENST00000342175.10:c.33308-41_33308-40insG (TTN)	ENSP00000340554.6:n.33308-41_33308-40insG
ENST00000342992.10:c.52223-41_52223-40insG (TTN)	ENSP00000343764.6:n.52223-41_52223-40insG
ENST00000359218.9:c.33107-41_33107-40insG (TTN)	ENSP00000352154.5:n.33107-41_33107-40insG
ENST00000460472.6:c.32732-41_32732-40insG (TTN)	ENSP00000434586.1:n.32732-41_32732-40insG
ENST00000589042.5:c.59927-41_59927-40insG (TTN) MANE Select	ENSP00000467141.1:n.59927-41_59927-40insG
ENST00000591111.5:c.55004-41_55004-40insG (TTN)	ENSP00000465570.1:n.55004-41_55004-40insG
ENST00000615779.4:c.55004-41_55004-40insG (TTN)	ENSP00000483597.1:n.55004-41_55004-40insG
NM_001256850.1:c.55004-41_55004-40insG (TTN)	NP_001243779.1:n.55004-41_55004-40insG
NM_001267550.2:c.59927-41_59927-40insG (TTN) MANE Select	NP_001254479.2:n.59927-41_59927-40insG
NM_003319.4:c.32732-41_32732-40insG (TTN)	NP_003310.4:n.32732-41_32732-40insG
NM_133378.4:c.52223-41_52223-40insG (TTN)	NP_596869.4:n.52223-41_52223-40insG
NM_133432.3:c.33107-41_33107-40insG (TTN)	NP_597676.3:n.33107-41_33107-40insG
NM_133437.4:c.33308-41_33308-40insG (TTN)	NP_597681.4:n.33308-41_33308-40insG
NR_038271.1:n.597-5664_597-5663insC (TTN-AS1)
NR_038272.1:n.3364+618_3364+619insC (TTN-AS1)
XM_011511729.1:c.59024-41_59024-40insG (TTN)	XP_011510031.1:n.59024-41_59024-40insG
XM_011511730.1:c.32918-41_32918-40insG (TTN)	XP_011510032.1:n.32918-41_32918-40insG
XM_011511731.1:c.32777-41_32777-40insG (TTN)	XP_011510033.1:n.32777-41_32777-40insG
XM_017004819.1:c.58820-41_58820-40insG (TTN)	XP_016860308.1:n.58820-41_58820-40insG
XM_017004820.1:c.54218-41_54218-40insG (TTN)	XP_016860309.1:n.54218-41_54218-40insG
XM_017004821.1:c.54215-41_54215-40insG (TTN)	XP_016860310.1:n.54215-41_54215-40insG
XM_017004822.1:c.51257-41_51257-40insG (TTN)	XP_016860311.1:n.51257-41_51257-40insG
XM_017004823.1:c.32873-41_32873-40insG (TTN)	XP_016860312.1:n.32873-41_32873-40insG
XM_024453094.1:c.54368-41_54368-40insG (TTN)	XP_024308862.1:n.54368-41_54368-40insG
XM_024453095.1:c.54365-41_54365-40insG (TTN)	XP_024308863.1:n.54365-41_54365-40insG
XM_024453096.1:c.53798-41_53798-40insG (TTN)	XP_024308864.1:n.53798-41_53798-40insG
XM_024453097.1:c.51140-41_51140-40insG (TTN)	XP_024308865.1:n.51140-41_51140-40insG
XM_024453098.1:c.51059-41_51059-40insG (TTN)	XP_024308866.1:n.51059-41_51059-40insG
XM_024453099.1:c.32822-41_32822-40insG (TTN)	XP_024308867.1:n.32822-41_32822-40insG
XM_024453100.1:c.22676-41_22676-40insG (TTN)	XP_024308868.1:n.22676-41_22676-40insG