Canonical Allele Identifier: CA538435461

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178581904dup , CM000664.2:g.178581904dup	GRCh38
NC_000002.11:g.179446631dup , CM000664.1:g.179446631dup	GRCh37
NC_000002.10:g.179154877dup	NCBI36
NG_011618.3:g.253899dup , LRG_391:g.253899dup
NG_051363.1:g.64078dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66463+2dup (TTN) MANE Select	NP_001254479.2:n.66463+2dup
ENST00000589042.5:c.66463+2dup (TTN) MANE Select	ENSP00000467141.1:n.66463+2dup
NM_001256850.1:c.61540+2dup (TTN)	NP_001243779.1:n.61540+2dup
NM_003319.4:c.39268+2dup (TTN)	NP_003310.4:n.39268+2dup
NM_133378.4:c.58759+2dup (TTN)	NP_596869.4:n.58759+2dup
NM_133432.3:c.39643+2dup (TTN)	NP_597676.3:n.39643+2dup
NM_133437.4:c.39844+2dup (TTN)	NP_597681.4:n.39844+2dup
NR_038271.1:n.596+10455dup (TTN-AS1)
NR_038272.1:n.2044-668dup (TTN-AS1)
ENST00000342175.10:c.39844+2dup (TTN)	ENSP00000340554.6:n.39844+2dup
ENST00000342175.11:c.39844+2dup (TTN)	ENSP00000340554.6:n.39844+2dup
ENST00000342992.10:c.58759+2dup (TTN)	ENSP00000343764.6:n.58759+2dup
ENST00000342992.11:c.58759+2dup (TTN)	ENSP00000343764.6:n.58759+2dup
ENST00000359218.10:c.39643+2dup (TTN)	ENSP00000352154.5:n.39643+2dup
ENST00000359218.9:c.39643+2dup (TTN)	ENSP00000352154.5:n.39643+2dup
ENST00000460472.6:c.39268+2dup (TTN)	ENSP00000434586.1:n.39268+2dup
ENST00000591111.5:c.61540+2dup (TTN)	ENSP00000465570.1:n.61540+2dup
ENST00000615779.4:c.61540+2dup (TTN)	ENSP00000483597.1:n.61540+2dup
XM_011511729.1:c.65560+2dup (TTN)	XP_011510031.1:n.65560+2dup
XM_011511730.1:c.39454+2dup (TTN)	XP_011510032.1:n.39454+2dup
XM_011511731.1:c.39313+2dup (TTN)	XP_011510033.1:n.39313+2dup
XM_017004819.1:c.65356+2dup (TTN)	XP_016860308.1:n.65356+2dup
XM_017004820.1:c.60754+2dup (TTN)	XP_016860309.1:n.60754+2dup
XM_017004821.1:c.60751+2dup (TTN)	XP_016860310.1:n.60751+2dup
XM_017004822.1:c.57793+2dup (TTN)	XP_016860311.1:n.57793+2dup
XM_017004823.1:c.39409+2dup (TTN)	XP_016860312.1:n.39409+2dup
XM_024453094.1:c.60904+2dup (TTN)	XP_024308862.1:n.60904+2dup
XM_024453095.1:c.60901+2dup (TTN)	XP_024308863.1:n.60901+2dup
XM_024453096.1:c.60334+2dup (TTN)	XP_024308864.1:n.60334+2dup
XM_024453097.1:c.57676+2dup (TTN)	XP_024308865.1:n.57676+2dup
XM_024453098.1:c.57595+2dup (TTN)	XP_024308866.1:n.57595+2dup
XM_024453099.1:c.39358+2dup (TTN)	XP_024308867.1:n.39358+2dup
XM_024453100.1:c.29212+2dup (TTN)	XP_024308868.1:n.29212+2dup