Canonical Allele Identifier: CA1985321

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178531577C>T , CM000664.2:g.178531577C>T	GRCh38
NC_000002.11:g.179396304C>T , CM000664.1:g.179396304C>T	GRCh37
NC_000002.10:g.179104550C>T	NCBI36
NG_011618.3:g.304226G>A , LRG_391:g.304226G>A
NG_051363.1:g.13751C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.105038G>A (TTN) MANE Select	NP_001254479.2:p.Arg35013His
ENST00000589042.5:c.105038G>A (TTN) MANE Select	ENSP00000467141.1:p.Arg35013His
NM_001256850.1:c.100115G>A (TTN)	NP_001243779.1:p.Arg33372His
NM_003319.4:c.77843G>A (TTN)	NP_003310.4:p.Arg25948His
NM_133378.4:c.97334G>A (TTN)	NP_596869.4:p.Arg32445His
NM_133432.3:c.78218G>A (TTN)	NP_597676.3:p.Arg26073His
NM_133437.4:c.78419G>A (TTN)	NP_597681.4:p.Arg26140His
NR_038271.1:n.446+7941C>T (TTN-AS1)
NR_038272.1:n.220-4155C>T (TTN-AS1)
ENST00000342175.10:c.78419G>A (TTN)	ENSP00000340554.6:p.Arg26140His
ENST00000342175.11:c.78419G>A (TTN)	ENSP00000340554.6:p.Arg26140His
ENST00000342992.10:c.97334G>A (TTN)	ENSP00000343764.6:p.Arg32445His
ENST00000342992.11:c.97334G>A (TTN)	ENSP00000343764.6:p.Arg32445His
ENST00000359218.10:c.78218G>A (TTN)	ENSP00000352154.5:p.Arg26073His
ENST00000359218.9:c.78218G>A (TTN)	ENSP00000352154.5:p.Arg26073His
ENST00000460472.6:c.77843G>A (TTN)	ENSP00000434586.1:p.Arg25948His
ENST00000591111.5:c.100115G>A (TTN)	ENSP00000465570.1:p.Arg33372His
ENST00000615779.4:c.100115G>A (TTN)	ENSP00000483597.1:p.Arg33372His
XM_011511729.1:c.104135G>A (TTN)	XP_011510031.1:p.Arg34712His
XM_011511730.1:c.78029G>A (TTN)	XP_011510032.1:p.Arg26010His
XM_011511731.1:c.77888G>A (TTN)	XP_011510033.1:p.Arg25963His
XM_017004819.1:c.103931G>A (TTN)	XP_016860308.1:p.Arg34644His
XM_017004820.1:c.99329G>A (TTN)	XP_016860309.1:p.Arg33110His
XM_017004821.1:c.99326G>A (TTN)	XP_016860310.1:p.Arg33109His
XM_017004822.1:c.96368G>A (TTN)	XP_016860311.1:p.Arg32123His
XM_017004823.1:c.77984G>A (TTN)	XP_016860312.1:p.Arg25995His
XM_024453094.1:c.99479G>A (TTN)	XP_024308862.1:p.Arg33160His
XM_024453095.1:c.99476G>A (TTN)	XP_024308863.1:p.Arg33159His
XM_024453096.1:c.98909G>A (TTN)	XP_024308864.1:p.Arg32970His
XM_024453097.1:c.96251G>A (TTN)	XP_024308865.1:p.Arg32084His
XM_024453098.1:c.96170G>A (TTN)	XP_024308866.1:p.Arg32057His
XM_024453099.1:c.77933G>A (TTN)	XP_024308867.1:p.Arg25978His
XM_024453100.1:c.67787G>A (TTN)	XP_024308868.1:p.Arg22596His