Canonical Allele Identifier: CA430111677

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178619727T>C , CM000664.2:g.178619727T>C	GRCh38
NC_000002.11:g.179484454T>C , CM000664.1:g.179484454T>C	GRCh37
NC_000002.10:g.179192699T>C	NCBI36
NG_011618.3:g.216076A>G , LRG_391:g.216076A>G
NG_051363.1:g.101901T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.46590A>G (TTN) MANE Select	NP_001254479.2:p.Glu15530=
ENST00000589042.5:c.46590A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu15530=
NM_001256850.1:c.41667A>G (TTN)	NP_001243779.1:p.Glu13889=
NM_003319.4:c.19395A>G (TTN)	NP_003310.4:p.Glu6465=
NM_133378.4:c.38886A>G (TTN)	NP_596869.4:p.Glu12962=
NM_133432.3:c.19770A>G (TTN)	NP_597676.3:p.Glu6590=
NM_133437.4:c.19971A>G (TTN)	NP_597681.4:p.Glu6657=
NR_038271.1:n.1605-26T>C (TTN-AS1)
ENST00000342175.10:c.19971A>G (TTN)	ENSP00000340554.6:p.Glu6657=
ENST00000342175.11:c.19971A>G (TTN)	ENSP00000340554.6:p.Glu6657=
ENST00000342992.10:c.38886A>G (TTN)	ENSP00000343764.6:p.Glu12962=
ENST00000342992.11:c.38886A>G (TTN)	ENSP00000343764.6:p.Glu12962=
ENST00000359218.10:c.19770A>G (TTN)	ENSP00000352154.5:p.Glu6590=
ENST00000359218.9:c.19770A>G (TTN)	ENSP00000352154.5:p.Glu6590=
ENST00000460472.6:c.19395A>G (TTN)	ENSP00000434586.1:p.Glu6465=
ENST00000591111.5:c.41667A>G (TTN)	ENSP00000465570.1:p.Glu13889=
ENST00000615779.4:c.41667A>G (TTN)	ENSP00000483597.1:p.Glu13889=
XM_011511729.1:c.45687A>G (TTN)	XP_011510031.1:p.Glu15229=
XM_011511730.1:c.19581A>G (TTN)	XP_011510032.1:p.Glu6527=
XM_011511731.1:c.19440A>G (TTN)	XP_011510033.1:p.Glu6480=
XM_017004819.1:c.45483A>G (TTN)	XP_016860308.1:p.Glu15161=
XM_017004820.1:c.40881A>G (TTN)	XP_016860309.1:p.Glu13627=
XM_017004821.1:c.40878A>G (TTN)	XP_016860310.1:p.Glu13626=
XM_017004822.1:c.37920A>G (TTN)	XP_016860311.1:p.Glu12640=
XM_017004823.1:c.19536A>G (TTN)	XP_016860312.1:p.Glu6512=
XM_024453094.1:c.41031A>G (TTN)	XP_024308862.1:p.Glu13677=
XM_024453095.1:c.41028A>G (TTN)	XP_024308863.1:p.Glu13676=
XM_024453096.1:c.40461A>G (TTN)	XP_024308864.1:p.Glu13487=
XM_024453097.1:c.37803A>G (TTN)	XP_024308865.1:p.Glu12601=
XM_024453098.1:c.37722A>G (TTN)	XP_024308866.1:p.Glu12574=
XM_024453099.1:c.19485A>G (TTN)	XP_024308867.1:p.Glu6495=
XM_024453100.1:c.9339A>G (TTN)	XP_024308868.1:p.Glu3113=