Canonical Allele Identifier: CA1310590186

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178713195_178713198delinsGTAT , CM000664.2:g.178713195_178713198delinsGTAT	GRCh38
NC_000002.11:g.179577922_179577925delinsGTAT , CM000664.1:g.179577922_179577925delinsGTAT	GRCh37
NC_000002.10:g.179286167_179286170delinsGTAT	NCBI36
NG_011618.3:g.122605_122608delinsATAC , LRG_391:g.122605_122608delinsATAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.23204_23207delinsATAC	ENSP00000343764.6:p.Asn7735=
ENST00000342175.11:c.13858+24884_13858+24887delinsATAC	ENSP00000340554.6:n.13858+24884_13858+24887delinsATAC
ENST00000359218.10:c.13657+24884_13657+24887delinsATAC	ENSP00000352154.5:n.13657+24884_13657+24887delinsATAC
ENST00000342175.10:c.13858+24884_13858+24887delinsATAC	ENSP00000340554.6:n.13858+24884_13858+24887delinsATAC
ENST00000342992.10:c.23204_23207delinsATAC	ENSP00000343764.6:p.Asn7735=
ENST00000359218.9:c.13657+24884_13657+24887delinsATAC	ENSP00000352154.5:n.13657+24884_13657+24887delinsATAC
ENST00000460472.6:c.13282+24884_13282+24887delinsATAC	ENSP00000434586.1:n.13282+24884_13282+24887delinsATAC
ENST00000589042.5:c.26936_26939delinsATAC MANE Select	ENSP00000467141.1:p.Asn8979=
ENST00000591111.5:c.25985_25988delinsATAC	ENSP00000465570.1:p.Asn8662=
ENST00000615779.4:c.25985_25988delinsATAC	ENSP00000483597.1:p.Asn8662=
NM_001256850.1:c.25985_25988delinsATAC	NP_001243779.1:p.Asn8662=
NM_001267550.2:c.26936_26939delinsATAC MANE Select	NP_001254479.2:p.Asn8979=
NM_003319.4:c.13282+24884_13282+24887delinsATAC	NP_003310.4:n.13282+24884_13282+24887delinsATAC
NM_133378.4:c.23204_23207delinsATAC	NP_596869.4:p.Asn7735=
NM_133432.3:c.13657+24884_13657+24887delinsATAC	NP_597676.3:n.13657+24884_13657+24887delinsATAC
NM_133437.4:c.13858+24884_13858+24887delinsATAC	NP_597681.4:n.13858+24884_13858+24887delinsATAC
XM_011511729.1:c.26033_26036delinsATAC	XP_011510031.1:p.Asn8678=
XM_011511730.1:c.13468+24884_13468+24887delinsATAC	XP_011510032.1:n.13468+24884_13468+24887delinsATAC
XM_011511731.1:c.13327+24884_13327+24887delinsATAC	XP_011510033.1:n.13327+24884_13327+24887delinsATAC
XM_017004819.1:c.25988_25991delinsATAC	XP_016860308.1:p.Asn8663=
XM_017004820.1:c.23207_23210delinsATAC	XP_016860309.1:p.Asn7736=
XM_017004821.1:c.23204_23207delinsATAC	XP_016860310.1:p.Asn7735=
XM_017004822.1:c.25988_25991delinsATAC	XP_016860311.1:p.Asn8663=
XM_017004823.1:c.13423+24884_13423+24887delinsATAC	XP_016860312.1:n.13423+24884_13423+24887delinsATAC
XM_024453094.1:c.25988_25991delinsATAC	XP_024308862.1:p.Asn8663=
XM_024453095.1:c.25988_25991delinsATAC	XP_024308863.1:p.Asn8663=
XM_024453096.1:c.25988_25991delinsATAC	XP_024308864.1:p.Asn8663=
XM_024453097.1:c.25988_25991delinsATAC	XP_024308865.1:p.Asn8663=
XM_024453098.1:c.25988_25991delinsATAC	XP_024308866.1:p.Asn8663=
XM_024453099.1:c.13423+24884_13423+24887delinsATAC	XP_024308867.1:n.13423+24884_13423+24887delinsATAC