Canonical Allele Identifier: CA1310514787

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530590_178530591delinsTA , CM000664.2:g.178530590_178530591delinsTA	GRCh38
NC_000002.11:g.179395317_179395318delinsTA , CM000664.1:g.179395317_179395318delinsTA	GRCh37
NC_000002.10:g.179103563_179103564delinsTA	NCBI36
NG_011618.3:g.305212_305213delinsTA , LRG_391:g.305212_305213delinsTA
NG_051363.1:g.12764_12765delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98320_98321delinsTA (TTN)	ENSP00000343764.6:p.Tyr32774=
ENST00000342175.11:c.79405_79406delinsTA (TTN)	ENSP00000340554.6:p.Tyr26469=
ENST00000359218.10:c.79204_79205delinsTA (TTN)	ENSP00000352154.5:p.Tyr26402=
ENST00000342175.10:c.79405_79406delinsTA (TTN)	ENSP00000340554.6:p.Tyr26469=
ENST00000342992.10:c.98320_98321delinsTA (TTN)	ENSP00000343764.6:p.Tyr32774=
ENST00000359218.9:c.79204_79205delinsTA (TTN)	ENSP00000352154.5:p.Tyr26402=
ENST00000460472.6:c.78829_78830delinsTA (TTN)	ENSP00000434586.1:p.Tyr26277=
ENST00000589042.5:c.106024_106025delinsTA (TTN) MANE Select	ENSP00000467141.1:p.Tyr35342=
ENST00000591111.5:c.101101_101102delinsTA (TTN)	ENSP00000465570.1:p.Tyr33701=
ENST00000615779.4:c.101101_101102delinsTA (TTN)	ENSP00000483597.1:p.Tyr33701=
NM_001256850.1:c.101101_101102delinsTA (TTN)	NP_001243779.1:p.Tyr33701=
NM_001267550.2:c.106024_106025delinsTA (TTN) MANE Select	NP_001254479.2:p.Tyr35342=
NM_003319.4:c.78829_78830delinsTA (TTN)	NP_003310.4:p.Tyr26277=
NM_133378.4:c.98320_98321delinsTA (TTN)	NP_596869.4:p.Tyr32774=
NM_133432.3:c.79204_79205delinsTA (TTN)	NP_597676.3:p.Tyr26402=
NM_133437.4:c.79405_79406delinsTA (TTN)	NP_597681.4:p.Tyr26469=
NR_038271.1:n.446+6954_446+6955delinsTA (TTN-AS1)
NR_038272.1:n.220-5142_220-5141delinsTA (TTN-AS1)
XM_011511729.1:c.105121_105122delinsTA (TTN)	XP_011510031.1:p.Tyr35041=
XM_011511730.1:c.79015_79016delinsTA (TTN)	XP_011510032.1:p.Tyr26339=
XM_011511731.1:c.78874_78875delinsTA (TTN)	XP_011510033.1:p.Tyr26292=
XM_017004819.1:c.104917_104918delinsTA (TTN)	XP_016860308.1:p.Tyr34973=
XM_017004820.1:c.100315_100316delinsTA (TTN)	XP_016860309.1:p.Tyr33439=
XM_017004821.1:c.100312_100313delinsTA (TTN)	XP_016860310.1:p.Tyr33438=
XM_017004822.1:c.97354_97355delinsTA (TTN)	XP_016860311.1:p.Tyr32452=
XM_017004823.1:c.78970_78971delinsTA (TTN)	XP_016860312.1:p.Tyr26324=
XM_024453094.1:c.100465_100466delinsTA (TTN)	XP_024308862.1:p.Tyr33489=
XM_024453095.1:c.100462_100463delinsTA (TTN)	XP_024308863.1:p.Tyr33488=
XM_024453096.1:c.99895_99896delinsTA (TTN)	XP_024308864.1:p.Tyr33299=
XM_024453097.1:c.97237_97238delinsTA (TTN)	XP_024308865.1:p.Tyr32413=
XM_024453098.1:c.97156_97157delinsTA (TTN)	XP_024308866.1:p.Tyr32386=
XM_024453099.1:c.78919_78920delinsTA (TTN)	XP_024308867.1:p.Tyr26307=
XM_024453100.1:c.68773_68774delinsTA (TTN)	XP_024308868.1:p.Tyr22925=