Canonical Allele Identifier: CA2662136090

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636402_178636404del , CM000664.2:g.178636402_178636404del	GRCh38
NC_000002.11:g.179501129_179501131del , CM000664.1:g.179501129_179501131del	GRCh37
NC_000002.10:g.179209374_179209376del	NCBI36
NG_011618.3:g.199400_199402del , LRG_391:g.199400_199402del

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.41324_41326del MANE Select	NP_001254479.2:p.Val13775del
ENST00000589042.5:c.41324_41326del MANE Select	ENSP00000467141.1:p.Val13775del
NM_001256850.1:c.36401_36403del	NP_001243779.1:p.Val12134del
NM_003319.4:c.14129_14131del	NP_003310.4:p.Val4710del
NM_133378.4:c.33620_33622del	NP_596869.4:p.Val11207del
NM_133432.3:c.14504_14506del	NP_597676.3:p.Val4835del
NM_133437.4:c.14705_14707del	NP_597681.4:p.Val4902del
ENST00000342175.10:c.14705_14707del	ENSP00000340554.6:p.Val4902del
ENST00000342175.11:c.14705_14707del	ENSP00000340554.6:p.Val4902del
ENST00000342992.10:c.33620_33622del	ENSP00000343764.6:p.Val11207del
ENST00000342992.11:c.33620_33622del	ENSP00000343764.6:p.Val11207del
ENST00000359218.10:c.14504_14506del	ENSP00000352154.5:p.Val4835del
ENST00000359218.9:c.14504_14506del	ENSP00000352154.5:p.Val4835del
ENST00000460472.6:c.14129_14131del	ENSP00000434586.1:p.Val4710del
ENST00000591111.5:c.36401_36403del	ENSP00000465570.1:p.Val12134del
ENST00000615779.4:c.36401_36403del	ENSP00000483597.1:p.Val12134del
XM_011511729.1:c.40421_40423del	XP_011510031.1:p.Val13474del
XM_011511730.1:c.14315_14317del	XP_011510032.1:p.Val4772del
XM_011511731.1:c.14174_14176del	XP_011510033.1:p.Val4725del
XM_017004819.1:c.40217_40219del	XP_016860308.1:p.Val13406del
XM_017004820.1:c.35615_35617del	XP_016860309.1:p.Val11872del
XM_017004821.1:c.35612_35614del	XP_016860310.1:p.Val11871del
XM_017004822.1:c.32654_32656del	XP_016860311.1:p.Val10885del
XM_017004823.1:c.14270_14272del	XP_016860312.1:p.Val4757del
XM_024453094.1:c.35765_35767del	XP_024308862.1:p.Val11922del
XM_024453095.1:c.35762_35764del	XP_024308863.1:p.Val11921del
XM_024453096.1:c.35195_35197del	XP_024308864.1:p.Val11732del
XM_024453097.1:c.32537_32539del	XP_024308865.1:p.Val10846del
XM_024453098.1:c.32456_32458del	XP_024308866.1:p.Val10819del
XM_024453099.1:c.14219_14221del	XP_024308867.1:p.Val4740del
XM_024453100.1:c.4073_4075del	XP_024308868.1:p.Val1358del