Canonical Allele Identifier: CA1986799

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543932A>C , CM000664.2:g.178543932A>C	GRCh38
NC_000002.11:g.179408659A>C , CM000664.1:g.179408659A>C	GRCh37
NC_000002.10:g.179116905A>C	NCBI36
NG_011618.3:g.291871T>G , LRG_391:g.291871T>G
NG_051363.1:g.26106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88508T>G (TTN)	ENSP00000343764.6:p.Ile29503Arg
ENST00000342175.11:c.69593T>G (TTN)	ENSP00000340554.6:p.Ile23198Arg
ENST00000359218.10:c.69392T>G (TTN)	ENSP00000352154.5:p.Ile23131Arg
ENST00000342175.10:c.69593T>G (TTN)	ENSP00000340554.6:p.Ile23198Arg
ENST00000342992.10:c.88508T>G (TTN)	ENSP00000343764.6:p.Ile29503Arg
ENST00000359218.9:c.69392T>G (TTN)	ENSP00000352154.5:p.Ile23131Arg
ENST00000460472.6:c.69017T>G (TTN)	ENSP00000434586.1:p.Ile23006Arg
ENST00000589042.5:c.96212T>G (TTN) MANE Select	ENSP00000467141.1:p.Ile32071Arg
ENST00000591111.5:c.91289T>G (TTN)	ENSP00000465570.1:p.Ile30430Arg
ENST00000615779.4:c.91289T>G (TTN)	ENSP00000483597.1:p.Ile30430Arg
NM_001256850.1:c.91289T>G (TTN)	NP_001243779.1:p.Ile30430Arg
NM_001267550.2:c.96212T>G (TTN) MANE Select	NP_001254479.2:p.Ile32071Arg
NM_003319.4:c.69017T>G (TTN)	NP_003310.4:p.Ile23006Arg
NM_133378.4:c.88508T>G (TTN)	NP_596869.4:p.Ile29503Arg
NM_133432.3:c.69392T>G (TTN)	NP_597676.3:p.Ile23131Arg
NM_133437.4:c.69593T>G (TTN)	NP_597681.4:p.Ile23198Arg
NR_038271.1:n.446+20296A>C (TTN-AS1)
NR_038272.1:n.2043+1571A>C (TTN-AS1)
XM_011511729.1:c.95309T>G (TTN)	XP_011510031.1:p.Ile31770Arg
XM_011511730.1:c.69203T>G (TTN)	XP_011510032.1:p.Ile23068Arg
XM_011511731.1:c.69062T>G (TTN)	XP_011510033.1:p.Ile23021Arg
XM_017004819.1:c.95105T>G (TTN)	XP_016860308.1:p.Ile31702Arg
XM_017004820.1:c.90503T>G (TTN)	XP_016860309.1:p.Ile30168Arg
XM_017004821.1:c.90500T>G (TTN)	XP_016860310.1:p.Ile30167Arg
XM_017004822.1:c.87542T>G (TTN)	XP_016860311.1:p.Ile29181Arg
XM_017004823.1:c.69158T>G (TTN)	XP_016860312.1:p.Ile23053Arg
XM_024453094.1:c.90653T>G (TTN)	XP_024308862.1:p.Ile30218Arg
XM_024453095.1:c.90650T>G (TTN)	XP_024308863.1:p.Ile30217Arg
XM_024453096.1:c.90083T>G (TTN)	XP_024308864.1:p.Ile30028Arg
XM_024453097.1:c.87425T>G (TTN)	XP_024308865.1:p.Ile29142Arg
XM_024453098.1:c.87344T>G (TTN)	XP_024308866.1:p.Ile29115Arg
XM_024453099.1:c.69107T>G (TTN)	XP_024308867.1:p.Ile23036Arg
XM_024453100.1:c.58961T>G (TTN)	XP_024308868.1:p.Ile19654Arg