Canonical Allele Identifier: CA2586970839

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614636_178614637insCAGT , CM000664.2:g.178614636_178614637insCAGT	GRCh38
NC_000002.11:g.179479363_179479364insCAGT , CM000664.1:g.179479363_179479364insCAGT	GRCh37
NC_000002.10:g.179187608_179187609insCAGT	NCBI36
NG_011618.3:g.221166_221167insACTG , LRG_391:g.221166_221167insACTG
NG_051363.1:g.96810_96811insCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41173_41174insACTG (TTN)	ENSP00000343764.6:p.Thr13725AsnfsTer5
ENST00000342175.11:c.22258_22259insACTG (TTN)	ENSP00000340554.6:p.Thr7420AsnfsTer5
ENST00000359218.10:c.22057_22058insACTG (TTN)	ENSP00000352154.5:p.Thr7353AsnfsTer5
ENST00000342175.10:c.22258_22259insACTG (TTN)	ENSP00000340554.6:p.Thr7420AsnfsTer5
ENST00000342992.10:c.41173_41174insACTG (TTN)	ENSP00000343764.6:p.Thr13725AsnfsTer5
ENST00000359218.9:c.22057_22058insACTG (TTN)	ENSP00000352154.5:p.Thr7353AsnfsTer5
ENST00000460472.6:c.21682_21683insACTG (TTN)	ENSP00000434586.1:p.Thr7228AsnfsTer5
ENST00000589042.5:c.48877_48878insACTG (TTN) MANE Select	ENSP00000467141.1:p.Thr16293AsnfsTer5
ENST00000591111.5:c.43954_43955insACTG (TTN)	ENSP00000465570.1:p.Thr14652AsnfsTer5
ENST00000615779.4:c.43954_43955insACTG (TTN)	ENSP00000483597.1:p.Thr14652AsnfsTer5
NM_001256850.1:c.43954_43955insACTG (TTN)	NP_001243779.1:p.Thr14652AsnfsTer5
NM_001267550.2:c.48877_48878insACTG (TTN) MANE Select	NP_001254479.2:p.Thr16293AsnfsTer5
NM_003319.4:c.21682_21683insACTG (TTN)	NP_003310.4:p.Thr7228AsnfsTer5
NM_133378.4:c.41173_41174insACTG (TTN)	NP_596869.4:p.Thr13725AsnfsTer5
NM_133432.3:c.22057_22058insACTG (TTN)	NP_597676.3:p.Thr7353AsnfsTer5
NM_133437.4:c.22258_22259insACTG (TTN)	NP_597681.4:p.Thr7420AsnfsTer5
NR_038271.1:n.1384_1385insCAGT (TTN-AS1)
XM_011511729.1:c.47974_47975insACTG (TTN)	XP_011510031.1:p.Thr15992AsnfsTer5
XM_011511730.1:c.21868_21869insACTG (TTN)	XP_011510032.1:p.Thr7290AsnfsTer5
XM_011511731.1:c.21727_21728insACTG (TTN)	XP_011510033.1:p.Thr7243AsnfsTer5
XM_017004819.1:c.47770_47771insACTG (TTN)	XP_016860308.1:p.Thr15924AsnfsTer5
XM_017004820.1:c.43168_43169insACTG (TTN)	XP_016860309.1:p.Thr14390AsnfsTer5
XM_017004821.1:c.43165_43166insACTG (TTN)	XP_016860310.1:p.Thr14389AsnfsTer5
XM_017004822.1:c.40207_40208insACTG (TTN)	XP_016860311.1:p.Thr13403AsnfsTer5
XM_017004823.1:c.21823_21824insACTG (TTN)	XP_016860312.1:p.Thr7275AsnfsTer5
XM_024453094.1:c.43318_43319insACTG (TTN)	XP_024308862.1:p.Thr14440AsnfsTer5
XM_024453095.1:c.43315_43316insACTG (TTN)	XP_024308863.1:p.Thr14439AsnfsTer5
XM_024453096.1:c.42748_42749insACTG (TTN)	XP_024308864.1:p.Thr14250AsnfsTer5
XM_024453097.1:c.40090_40091insACTG (TTN)	XP_024308865.1:p.Thr13364AsnfsTer5
XM_024453098.1:c.40009_40010insACTG (TTN)	XP_024308866.1:p.Thr13337AsnfsTer5
XM_024453099.1:c.21772_21773insACTG (TTN)	XP_024308867.1:p.Thr7258AsnfsTer5
XM_024453100.1:c.11626_11627insACTG (TTN)	XP_024308868.1:p.Thr3876AsnfsTer5