Canonical Allele Identifier: CA2753332597

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591900_178591901del , CM000664.2:g.178591900_178591901del	GRCh38
NC_000002.11:g.179456627_179456628del , CM000664.1:g.179456627_179456628del	GRCh37
NC_000002.10:g.179164873_179164874del	NCBI36
NG_011618.3:g.243903_243904del , LRG_391:g.243903_243904del
NG_051363.1:g.74074_74075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52223-8_52223-7del (TTN)	ENSP00000343764.6:n.52223-8_52223-7del
ENST00000342175.11:c.33308-8_33308-7del (TTN)	ENSP00000340554.6:n.33308-8_33308-7del
ENST00000359218.10:c.33107-8_33107-7del (TTN)	ENSP00000352154.5:n.33107-8_33107-7del
ENST00000342175.10:c.33308-8_33308-7del (TTN)	ENSP00000340554.6:n.33308-8_33308-7del
ENST00000342992.10:c.52223-8_52223-7del (TTN)	ENSP00000343764.6:n.52223-8_52223-7del
ENST00000359218.9:c.33107-8_33107-7del (TTN)	ENSP00000352154.5:n.33107-8_33107-7del
ENST00000460472.6:c.32732-8_32732-7del (TTN)	ENSP00000434586.1:n.32732-8_32732-7del
ENST00000589042.5:c.59927-8_59927-7del (TTN) MANE Select	ENSP00000467141.1:n.59927-8_59927-7del
ENST00000591111.5:c.55004-8_55004-7del (TTN)	ENSP00000465570.1:n.55004-8_55004-7del
ENST00000615779.4:c.55004-8_55004-7del (TTN)	ENSP00000483597.1:n.55004-8_55004-7del
NM_001256850.1:c.55004-8_55004-7del (TTN)	NP_001243779.1:n.55004-8_55004-7del
NM_001267550.2:c.59927-8_59927-7del (TTN) MANE Select	NP_001254479.2:n.59927-8_59927-7del
NM_003319.4:c.32732-8_32732-7del (TTN)	NP_003310.4:n.32732-8_32732-7del
NM_133378.4:c.52223-8_52223-7del (TTN)	NP_596869.4:n.52223-8_52223-7del
NM_133432.3:c.33107-8_33107-7del (TTN)	NP_597676.3:n.33107-8_33107-7del
NM_133437.4:c.33308-8_33308-7del (TTN)	NP_597681.4:n.33308-8_33308-7del
NR_038271.1:n.597-5696_597-5695del (TTN-AS1)
NR_038272.1:n.3364+586_3364+587del (TTN-AS1)
XM_011511729.1:c.59024-8_59024-7del (TTN)	XP_011510031.1:n.59024-8_59024-7del
XM_011511730.1:c.32918-8_32918-7del (TTN)	XP_011510032.1:n.32918-8_32918-7del
XM_011511731.1:c.32777-8_32777-7del (TTN)	XP_011510033.1:n.32777-8_32777-7del
XM_017004819.1:c.58820-8_58820-7del (TTN)	XP_016860308.1:n.58820-8_58820-7del
XM_017004820.1:c.54218-8_54218-7del (TTN)	XP_016860309.1:n.54218-8_54218-7del
XM_017004821.1:c.54215-8_54215-7del (TTN)	XP_016860310.1:n.54215-8_54215-7del
XM_017004822.1:c.51257-8_51257-7del (TTN)	XP_016860311.1:n.51257-8_51257-7del
XM_017004823.1:c.32873-8_32873-7del (TTN)	XP_016860312.1:n.32873-8_32873-7del
XM_024453094.1:c.54368-8_54368-7del (TTN)	XP_024308862.1:n.54368-8_54368-7del
XM_024453095.1:c.54365-8_54365-7del (TTN)	XP_024308863.1:n.54365-8_54365-7del
XM_024453096.1:c.53798-8_53798-7del (TTN)	XP_024308864.1:n.53798-8_53798-7del
XM_024453097.1:c.51140-8_51140-7del (TTN)	XP_024308865.1:n.51140-8_51140-7del
XM_024453098.1:c.51059-8_51059-7del (TTN)	XP_024308866.1:n.51059-8_51059-7del
XM_024453099.1:c.32822-8_32822-7del (TTN)	XP_024308867.1:n.32822-8_32822-7del
XM_024453100.1:c.22676-8_22676-7del (TTN)	XP_024308868.1:n.22676-8_22676-7del