Canonical Allele Identifier: CA349487471

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178548473A>C , CM000664.2:g.178548473A>C	GRCh38
NC_000002.11:g.179413200A>C , CM000664.1:g.179413200A>C	GRCh37
NC_000002.10:g.179121446A>C	NCBI36
NG_011618.3:g.287330T>G , LRG_391:g.287330T>G
NG_051363.1:g.30647A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.93153T>G (TTN) MANE Select	NP_001254479.2:p.Tyr31051Ter
ENST00000589042.5:c.93153T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr31051Ter
NM_001256850.1:c.88230T>G (TTN)	NP_001243779.1:p.Tyr29410Ter
NM_003319.4:c.65958T>G (TTN)	NP_003310.4:p.Tyr21986Ter
NM_133378.4:c.85449T>G (TTN)	NP_596869.4:p.Tyr28483Ter
NM_133432.3:c.66333T>G (TTN)	NP_597676.3:p.Tyr22111Ter
NM_133437.4:c.66534T>G (TTN)	NP_597681.4:p.Tyr22178Ter
NR_038271.1:n.447-22827A>C (TTN-AS1)
NR_038272.1:n.2043+6112A>C (TTN-AS1)
ENST00000342175.10:c.66534T>G (TTN)	ENSP00000340554.6:p.Tyr22178Ter
ENST00000342175.11:c.66534T>G (TTN)	ENSP00000340554.6:p.Tyr22178Ter
ENST00000342992.10:c.85449T>G (TTN)	ENSP00000343764.6:p.Tyr28483Ter
ENST00000342992.11:c.85449T>G (TTN)	ENSP00000343764.6:p.Tyr28483Ter
ENST00000359218.10:c.66333T>G (TTN)	ENSP00000352154.5:p.Tyr22111Ter
ENST00000359218.9:c.66333T>G (TTN)	ENSP00000352154.5:p.Tyr22111Ter
ENST00000460472.6:c.65958T>G (TTN)	ENSP00000434586.1:p.Tyr21986Ter
ENST00000591111.5:c.88230T>G (TTN)	ENSP00000465570.1:p.Tyr29410Ter
ENST00000615779.4:c.88230T>G (TTN)	ENSP00000483597.1:p.Tyr29410Ter
XM_011511729.1:c.92250T>G (TTN)	XP_011510031.1:p.Tyr30750Ter
XM_011511730.1:c.66144T>G (TTN)	XP_011510032.1:p.Tyr22048Ter
XM_011511731.1:c.66003T>G (TTN)	XP_011510033.1:p.Tyr22001Ter
XM_017004819.1:c.92046T>G (TTN)	XP_016860308.1:p.Tyr30682Ter
XM_017004820.1:c.87444T>G (TTN)	XP_016860309.1:p.Tyr29148Ter
XM_017004821.1:c.87441T>G (TTN)	XP_016860310.1:p.Tyr29147Ter
XM_017004822.1:c.84483T>G (TTN)	XP_016860311.1:p.Tyr28161Ter
XM_017004823.1:c.66099T>G (TTN)	XP_016860312.1:p.Tyr22033Ter
XM_024453094.1:c.87594T>G (TTN)	XP_024308862.1:p.Tyr29198Ter
XM_024453095.1:c.87591T>G (TTN)	XP_024308863.1:p.Tyr29197Ter
XM_024453096.1:c.87024T>G (TTN)	XP_024308864.1:p.Tyr29008Ter
XM_024453097.1:c.84366T>G (TTN)	XP_024308865.1:p.Tyr28122Ter
XM_024453098.1:c.84285T>G (TTN)	XP_024308866.1:p.Tyr28095Ter
XM_024453099.1:c.66048T>G (TTN)	XP_024308867.1:p.Tyr22016Ter
XM_024453100.1:c.55902T>G (TTN)	XP_024308868.1:p.Tyr18634Ter