Canonical Allele Identifier: CA1310514757

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530565_178530566delinsAG , CM000664.2:g.178530565_178530566delinsAG	GRCh38
NC_000002.11:g.179395292_179395293delinsAG , CM000664.1:g.179395292_179395293delinsAG	GRCh37
NC_000002.10:g.179103538_179103539delinsAG	NCBI36
NG_011618.3:g.305237_305238delinsCT , LRG_391:g.305237_305238delinsCT
NG_051363.1:g.12739_12740delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98345_98346delinsCT (TTN)	ENSP00000343764.6:p.Thr32782=
ENST00000342175.11:c.79430_79431delinsCT (TTN)	ENSP00000340554.6:p.Thr26477=
ENST00000359218.10:c.79229_79230delinsCT (TTN)	ENSP00000352154.5:p.Thr26410=
ENST00000342175.10:c.79430_79431delinsCT (TTN)	ENSP00000340554.6:p.Thr26477=
ENST00000342992.10:c.98345_98346delinsCT (TTN)	ENSP00000343764.6:p.Thr32782=
ENST00000359218.9:c.79229_79230delinsCT (TTN)	ENSP00000352154.5:p.Thr26410=
ENST00000460472.6:c.78854_78855delinsCT (TTN)	ENSP00000434586.1:p.Thr26285=
ENST00000589042.5:c.106049_106050delinsCT (TTN) MANE Select	ENSP00000467141.1:p.Thr35350=
ENST00000591111.5:c.101126_101127delinsCT (TTN)	ENSP00000465570.1:p.Thr33709=
ENST00000615779.4:c.101126_101127delinsCT (TTN)	ENSP00000483597.1:p.Thr33709=
NM_001256850.1:c.101126_101127delinsCT (TTN)	NP_001243779.1:p.Thr33709=
NM_001267550.2:c.106049_106050delinsCT (TTN) MANE Select	NP_001254479.2:p.Thr35350=
NM_003319.4:c.78854_78855delinsCT (TTN)	NP_003310.4:p.Thr26285=
NM_133378.4:c.98345_98346delinsCT (TTN)	NP_596869.4:p.Thr32782=
NM_133432.3:c.79229_79230delinsCT (TTN)	NP_597676.3:p.Thr26410=
NM_133437.4:c.79430_79431delinsCT (TTN)	NP_597681.4:p.Thr26477=
NR_038271.1:n.446+6929_446+6930delinsAG (TTN-AS1)
NR_038272.1:n.220-5167_220-5166delinsAG (TTN-AS1)
XM_011511729.1:c.105146_105147delinsCT (TTN)	XP_011510031.1:p.Thr35049=
XM_011511730.1:c.79040_79041delinsCT (TTN)	XP_011510032.1:p.Thr26347=
XM_011511731.1:c.78899_78900delinsCT (TTN)	XP_011510033.1:p.Thr26300=
XM_017004819.1:c.104942_104943delinsCT (TTN)	XP_016860308.1:p.Thr34981=
XM_017004820.1:c.100340_100341delinsCT (TTN)	XP_016860309.1:p.Thr33447=
XM_017004821.1:c.100337_100338delinsCT (TTN)	XP_016860310.1:p.Thr33446=
XM_017004822.1:c.97379_97380delinsCT (TTN)	XP_016860311.1:p.Thr32460=
XM_017004823.1:c.78995_78996delinsCT (TTN)	XP_016860312.1:p.Thr26332=
XM_024453094.1:c.100490_100491delinsCT (TTN)	XP_024308862.1:p.Thr33497=
XM_024453095.1:c.100487_100488delinsCT (TTN)	XP_024308863.1:p.Thr33496=
XM_024453096.1:c.99920_99921delinsCT (TTN)	XP_024308864.1:p.Thr33307=
XM_024453097.1:c.97262_97263delinsCT (TTN)	XP_024308865.1:p.Thr32421=
XM_024453098.1:c.97181_97182delinsCT (TTN)	XP_024308866.1:p.Thr32394=
XM_024453099.1:c.78944_78945delinsCT (TTN)	XP_024308867.1:p.Thr26315=
XM_024453100.1:c.68798_68799delinsCT (TTN)	XP_024308868.1:p.Thr22933=