Canonical Allele Identifier: CA2538156308

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689226_178689227del , CM000664.2:g.178689226_178689227del	GRCh38
NC_000002.11:g.179553953_179553954del , CM000664.1:g.179553953_179553954del	GRCh37
NC_000002.10:g.179262198_179262199del	NCBI36
NG_011618.3:g.146578_146579del , LRG_391:g.146578_146579del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.28279+65_28279+66del	ENSP00000343764.6:n.28279+65_28279+66del
ENST00000342175.11:c.13859-46908_13859-46907del	ENSP00000340554.6:n.13859-46908_13859-46907del
ENST00000359218.10:c.13658-46908_13658-46907del	ENSP00000352154.5:n.13658-46908_13658-46907del
ENST00000342175.10:c.13859-46908_13859-46907del	ENSP00000340554.6:n.13859-46908_13859-46907del
ENST00000342992.10:c.28279+65_28279+66del	ENSP00000343764.6:n.28279+65_28279+66del
ENST00000359218.9:c.13658-46908_13658-46907del	ENSP00000352154.5:n.13658-46908_13658-46907del
ENST00000414766.5:c.1645+65_1645+66del	ENSP00000401501.1:n.1645+65_1645+66del
ENST00000460472.6:c.13283-46908_13283-46907del	ENSP00000434586.1:n.13283-46908_13283-46907del
ENST00000589042.5:c.32011+65_32011+66del MANE Select	ENSP00000467141.1:n.32011+65_32011+66del
ENST00000591111.5:c.31060+65_31060+66del	ENSP00000465570.1:n.31060+65_31060+66del
ENST00000615779.4:c.31060+65_31060+66del	ENSP00000483597.1:n.31060+65_31060+66del
NM_001256850.1:c.31060+65_31060+66del	NP_001243779.1:n.31060+65_31060+66del
NM_001267550.2:c.32011+65_32011+66del MANE Select	NP_001254479.2:n.32011+65_32011+66del
NM_003319.4:c.13283-46908_13283-46907del	NP_003310.4:n.13283-46908_13283-46907del
NM_133378.4:c.28279+65_28279+66del	NP_596869.4:n.28279+65_28279+66del
NM_133432.3:c.13658-46908_13658-46907del	NP_597676.3:n.13658-46908_13658-46907del
NM_133437.4:c.13859-46908_13859-46907del	NP_597681.4:n.13859-46908_13859-46907del
XM_011511729.1:c.31108+65_31108+66del	XP_011510031.1:n.31108+65_31108+66del
XM_011511730.1:c.13469-46908_13469-46907del	XP_011510032.1:n.13469-46908_13469-46907del
XM_011511731.1:c.13328-46908_13328-46907del	XP_011510033.1:n.13328-46908_13328-46907del
XM_017004819.1:c.31063+65_31063+66del	XP_016860308.1:n.31063+65_31063+66del
XM_017004820.1:c.28282+65_28282+66del	XP_016860309.1:n.28282+65_28282+66del
XM_017004821.1:c.28279+65_28279+66del	XP_016860310.1:n.28279+65_28279+66del
XM_017004822.1:c.31063+65_31063+66del	XP_016860311.1:n.31063+65_31063+66del
XM_017004823.1:c.13424-46908_13424-46907del	XP_016860312.1:n.13424-46908_13424-46907del
XM_024453094.1:c.31063+65_31063+66del	XP_024308862.1:n.31063+65_31063+66del
XM_024453095.1:c.31063+65_31063+66del	XP_024308863.1:n.31063+65_31063+66del
XM_024453096.1:c.31063+65_31063+66del	XP_024308864.1:n.31063+65_31063+66del
XM_024453097.1:c.30898+588_30898+589del	XP_024308865.1:n.30898+588_30898+589del
XM_024453098.1:c.30898+588_30898+589del	XP_024308866.1:n.30898+588_30898+589del
XM_024453099.1:c.13424-46908_13424-46907del	XP_024308867.1:n.13424-46908_13424-46907del