Canonical Allele Identifier: CA2662142688

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178672519_178672520dup , CM000664.2:g.178672519_178672520dup	GRCh38
NC_000002.11:g.179537246_179537247dup , CM000664.1:g.179537246_179537247dup	GRCh37
NC_000002.10:g.179245491_179245492dup	NCBI36
NG_011618.3:g.163286_163287dup , LRG_391:g.163286_163287dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.34856-36_34856-35dup MANE Select	NP_001254479.2:n.34856-36_34856-35dup
ENST00000589042.5:c.34856-36_34856-35dup MANE Select	ENSP00000467141.1:n.34856-36_34856-35dup
NM_001256850.1:c.33734-36_33734-35dup	NP_001243779.1:n.33734-36_33734-35dup
NM_003319.4:c.13283-30200_13283-30199dup	NP_003310.4:n.13283-30200_13283-30199dup
NM_133378.4:c.30953-36_30953-35dup	NP_596869.4:n.30953-36_30953-35dup
NM_133432.3:c.13658-30200_13658-30199dup	NP_597676.3:n.13658-30200_13658-30199dup
NM_133437.4:c.13859-30200_13859-30199dup	NP_597681.4:n.13859-30200_13859-30199dup
ENST00000342175.10:c.13859-30200_13859-30199dup	ENSP00000340554.6:n.13859-30200_13859-30199dup
ENST00000342175.11:c.13859-30200_13859-30199dup	ENSP00000340554.6:n.13859-30200_13859-30199dup
ENST00000342992.10:c.30953-36_30953-35dup	ENSP00000343764.6:n.30953-36_30953-35dup
ENST00000342992.11:c.30953-36_30953-35dup	ENSP00000343764.6:n.30953-36_30953-35dup
ENST00000359218.10:c.13658-30200_13658-30199dup	ENSP00000352154.5:n.13658-30200_13658-30199dup
ENST00000359218.9:c.13658-30200_13658-30199dup	ENSP00000352154.5:n.13658-30200_13658-30199dup
ENST00000414766.5:c.2440+1116_2440+1117dup	ENSP00000401501.1:n.2440+1116_2440+1117dup
ENST00000460472.6:c.13283-30200_13283-30199dup	ENSP00000434586.1:n.13283-30200_13283-30199dup
ENST00000591111.5:c.33734-36_33734-35dup	ENSP00000465570.1:n.33734-36_33734-35dup
ENST00000615779.4:c.33734-36_33734-35dup	ENSP00000483597.1:n.33734-36_33734-35dup
XM_011511729.1:c.33953-36_33953-35dup	XP_011510031.1:n.33953-36_33953-35dup
XM_011511730.1:c.13469-30200_13469-30199dup	XP_011510032.1:n.13469-30200_13469-30199dup
XM_011511731.1:c.13328-30200_13328-30199dup	XP_011510033.1:n.13328-30200_13328-30199dup
XM_017004819.1:c.33908-36_33908-35dup	XP_016860308.1:n.33908-36_33908-35dup
XM_017004820.1:c.30956-36_30956-35dup	XP_016860309.1:n.30956-36_30956-35dup
XM_017004821.1:c.30953-36_30953-35dup	XP_016860310.1:n.30953-36_30953-35dup
XM_017004822.1:c.31858+1116_31858+1117dup	XP_016860311.1:n.31858+1116_31858+1117dup
XM_017004823.1:c.13424-30200_13424-30199dup	XP_016860312.1:n.13424-30200_13424-30199dup
XM_024453094.1:c.33220+1116_33220+1117dup	XP_024308862.1:n.33220+1116_33220+1117dup
XM_024453095.1:c.33295+1116_33295+1117dup	XP_024308863.1:n.33295+1116_33295+1117dup
XM_024453096.1:c.32650+1116_32650+1117dup	XP_024308864.1:n.32650+1116_32650+1117dup
XM_024453097.1:c.31690+1116_31690+1117dup	XP_024308865.1:n.31690+1116_31690+1117dup
XM_024453098.1:c.31609+1116_31609+1117dup	XP_024308866.1:n.31609+1116_31609+1117dup
XM_024453099.1:c.13424-30200_13424-30199dup	XP_024308867.1:n.13424-30200_13424-30199dup