Canonical Allele Identifier: CA2753333580

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178566257_178566258insCGCCT , CM000664.2:g.178566257_178566258insCGCCT	GRCh38
NC_000002.11:g.179430984_179430985insCGCCT , CM000664.1:g.179430984_179430985insCGCCT	GRCh37
NC_000002.10:g.179139230_179139231insCGCCT	NCBI36
NG_011618.3:g.269545_269546insAGGCG , LRG_391:g.269545_269546insAGGCG
NG_051363.1:g.48431_48432insCGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.72170_72171insAGGCG (TTN)	ENSP00000343764.6:p.Trp24058GlyfsTer20
ENST00000342175.11:c.53255_53256insAGGCG (TTN)	ENSP00000340554.6:p.Trp17753GlyfsTer20
ENST00000359218.10:c.53054_53055insAGGCG (TTN)	ENSP00000352154.5:p.Trp17686GlyfsTer20
ENST00000342175.10:c.53255_53256insAGGCG (TTN)	ENSP00000340554.6:p.Trp17753GlyfsTer20
ENST00000342992.10:c.72170_72171insAGGCG (TTN)	ENSP00000343764.6:p.Trp24058GlyfsTer20
ENST00000359218.9:c.53054_53055insAGGCG (TTN)	ENSP00000352154.5:p.Trp17686GlyfsTer20
ENST00000460472.6:c.52679_52680insAGGCG (TTN)	ENSP00000434586.1:p.Trp17561GlyfsTer20
ENST00000589042.5:c.79874_79875insAGGCG (TTN) MANE Select	ENSP00000467141.1:p.Trp26626GlyfsTer20
ENST00000591111.5:c.74951_74952insAGGCG (TTN)	ENSP00000465570.1:p.Trp24985GlyfsTer20
ENST00000615779.4:c.74951_74952insAGGCG (TTN)	ENSP00000483597.1:p.Trp24985GlyfsTer20
NM_001256850.1:c.74951_74952insAGGCG (TTN)	NP_001243779.1:p.Trp24985GlyfsTer20
NM_001267550.2:c.79874_79875insAGGCG (TTN) MANE Select	NP_001254479.2:p.Trp26626GlyfsTer20
NM_003319.4:c.52679_52680insAGGCG (TTN)	NP_003310.4:p.Trp17561GlyfsTer20
NM_133378.4:c.72170_72171insAGGCG (TTN)	NP_596869.4:p.Trp24058GlyfsTer20
NM_133432.3:c.53054_53055insAGGCG (TTN)	NP_597676.3:p.Trp17686GlyfsTer20
NM_133437.4:c.53255_53256insAGGCG (TTN)	NP_597681.4:p.Trp17753GlyfsTer20
NR_038271.1:n.447-5043_447-5042insCGCCT (TTN-AS1)
NR_038272.1:n.2044-16315_2044-16314insCGCCT (TTN-AS1)
XM_011511729.1:c.78971_78972insAGGCG (TTN)	XP_011510031.1:p.Trp26325GlyfsTer20
XM_011511730.1:c.52865_52866insAGGCG (TTN)	XP_011510032.1:p.Trp17623GlyfsTer20
XM_011511731.1:c.52724_52725insAGGCG (TTN)	XP_011510033.1:p.Trp17576GlyfsTer20
XM_017004819.1:c.78767_78768insAGGCG (TTN)	XP_016860308.1:p.Trp26257GlyfsTer20
XM_017004820.1:c.74165_74166insAGGCG (TTN)	XP_016860309.1:p.Trp24723GlyfsTer20
XM_017004821.1:c.74162_74163insAGGCG (TTN)	XP_016860310.1:p.Trp24722GlyfsTer20
XM_017004822.1:c.71204_71205insAGGCG (TTN)	XP_016860311.1:p.Trp23736GlyfsTer20
XM_017004823.1:c.52820_52821insAGGCG (TTN)	XP_016860312.1:p.Trp17608GlyfsTer20
XM_024453094.1:c.74315_74316insAGGCG (TTN)	XP_024308862.1:p.Trp24773GlyfsTer20
XM_024453095.1:c.74312_74313insAGGCG (TTN)	XP_024308863.1:p.Trp24772GlyfsTer20
XM_024453096.1:c.73745_73746insAGGCG (TTN)	XP_024308864.1:p.Trp24583GlyfsTer20
XM_024453097.1:c.71087_71088insAGGCG (TTN)	XP_024308865.1:p.Trp23697GlyfsTer20
XM_024453098.1:c.71006_71007insAGGCG (TTN)	XP_024308866.1:p.Trp23670GlyfsTer20
XM_024453099.1:c.52769_52770insAGGCG (TTN)	XP_024308867.1:p.Trp17591GlyfsTer20
XM_024453100.1:c.42623_42624insAGGCG (TTN)	XP_024308868.1:p.Trp14209GlyfsTer20