Canonical Allele Identifier: CA349447685

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543448G>C , CM000664.2:g.178543448G>C	GRCh38
NC_000002.11:g.179408175G>C , CM000664.1:g.179408175G>C	GRCh37
NC_000002.10:g.179116421G>C	NCBI36
NG_011618.3:g.292355C>G , LRG_391:g.292355C>G
NG_051363.1:g.25622G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.96525C>G (TTN) MANE Select	NP_001254479.2:p.Tyr32175Ter
ENST00000589042.5:c.96525C>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr32175Ter
NM_001256850.1:c.91602C>G (TTN)	NP_001243779.1:p.Tyr30534Ter
NM_003319.4:c.69330C>G (TTN)	NP_003310.4:p.Tyr23110Ter
NM_133378.4:c.88821C>G (TTN)	NP_596869.4:p.Tyr29607Ter
NM_133432.3:c.69705C>G (TTN)	NP_597676.3:p.Tyr23235Ter
NM_133437.4:c.69906C>G (TTN)	NP_597681.4:p.Tyr23302Ter
NR_038271.1:n.446+19812G>C (TTN-AS1)
NR_038272.1:n.2043+1087G>C (TTN-AS1)
ENST00000342175.10:c.69906C>G (TTN)	ENSP00000340554.6:p.Tyr23302Ter
ENST00000342175.11:c.69906C>G (TTN)	ENSP00000340554.6:p.Tyr23302Ter
ENST00000342992.10:c.88821C>G (TTN)	ENSP00000343764.6:p.Tyr29607Ter
ENST00000342992.11:c.88821C>G (TTN)	ENSP00000343764.6:p.Tyr29607Ter
ENST00000359218.10:c.69705C>G (TTN)	ENSP00000352154.5:p.Tyr23235Ter
ENST00000359218.9:c.69705C>G (TTN)	ENSP00000352154.5:p.Tyr23235Ter
ENST00000460472.6:c.69330C>G (TTN)	ENSP00000434586.1:p.Tyr23110Ter
ENST00000591111.5:c.91602C>G (TTN)	ENSP00000465570.1:p.Tyr30534Ter
ENST00000615779.4:c.91602C>G (TTN)	ENSP00000483597.1:p.Tyr30534Ter
XM_011511729.1:c.95622C>G (TTN)	XP_011510031.1:p.Tyr31874Ter
XM_011511730.1:c.69516C>G (TTN)	XP_011510032.1:p.Tyr23172Ter
XM_011511731.1:c.69375C>G (TTN)	XP_011510033.1:p.Tyr23125Ter
XM_017004819.1:c.95418C>G (TTN)	XP_016860308.1:p.Tyr31806Ter
XM_017004820.1:c.90816C>G (TTN)	XP_016860309.1:p.Tyr30272Ter
XM_017004821.1:c.90813C>G (TTN)	XP_016860310.1:p.Tyr30271Ter
XM_017004822.1:c.87855C>G (TTN)	XP_016860311.1:p.Tyr29285Ter
XM_017004823.1:c.69471C>G (TTN)	XP_016860312.1:p.Tyr23157Ter
XM_024453094.1:c.90966C>G (TTN)	XP_024308862.1:p.Tyr30322Ter
XM_024453095.1:c.90963C>G (TTN)	XP_024308863.1:p.Tyr30321Ter
XM_024453096.1:c.90396C>G (TTN)	XP_024308864.1:p.Tyr30132Ter
XM_024453097.1:c.87738C>G (TTN)	XP_024308865.1:p.Tyr29246Ter
XM_024453098.1:c.87657C>G (TTN)	XP_024308866.1:p.Tyr29219Ter
XM_024453099.1:c.69420C>G (TTN)	XP_024308867.1:p.Tyr23140Ter
XM_024453100.1:c.59274C>G (TTN)	XP_024308868.1:p.Tyr19758Ter