Canonical Allele Identifier: CA349473827

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547073A>C , CM000664.2:g.178547073A>C	GRCh38
NC_000002.11:g.179411800A>C , CM000664.1:g.179411800A>C	GRCh37
NC_000002.10:g.179120046A>C	NCBI36
NG_011618.3:g.288730T>G , LRG_391:g.288730T>G
NG_051363.1:g.29247A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.94452T>G (TTN) MANE Select	NP_001254479.2:p.Tyr31484Ter
ENST00000589042.5:c.94452T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr31484Ter
NM_001256850.1:c.89529T>G (TTN)	NP_001243779.1:p.Tyr29843Ter
NM_003319.4:c.67257T>G (TTN)	NP_003310.4:p.Tyr22419Ter
NM_133378.4:c.86748T>G (TTN)	NP_596869.4:p.Tyr28916Ter
NM_133432.3:c.67632T>G (TTN)	NP_597676.3:p.Tyr22544Ter
NM_133437.4:c.67833T>G (TTN)	NP_597681.4:p.Tyr22611Ter
NR_038271.1:n.446+23437A>C (TTN-AS1)
NR_038272.1:n.2043+4712A>C (TTN-AS1)
ENST00000342175.10:c.67833T>G (TTN)	ENSP00000340554.6:p.Tyr22611Ter
ENST00000342175.11:c.67833T>G (TTN)	ENSP00000340554.6:p.Tyr22611Ter
ENST00000342992.10:c.86748T>G (TTN)	ENSP00000343764.6:p.Tyr28916Ter
ENST00000342992.11:c.86748T>G (TTN)	ENSP00000343764.6:p.Tyr28916Ter
ENST00000359218.10:c.67632T>G (TTN)	ENSP00000352154.5:p.Tyr22544Ter
ENST00000359218.9:c.67632T>G (TTN)	ENSP00000352154.5:p.Tyr22544Ter
ENST00000460472.6:c.67257T>G (TTN)	ENSP00000434586.1:p.Tyr22419Ter
ENST00000591111.5:c.89529T>G (TTN)	ENSP00000465570.1:p.Tyr29843Ter
ENST00000615779.4:c.89529T>G (TTN)	ENSP00000483597.1:p.Tyr29843Ter
XM_011511729.1:c.93549T>G (TTN)	XP_011510031.1:p.Tyr31183Ter
XM_011511730.1:c.67443T>G (TTN)	XP_011510032.1:p.Tyr22481Ter
XM_011511731.1:c.67302T>G (TTN)	XP_011510033.1:p.Tyr22434Ter
XM_017004819.1:c.93345T>G (TTN)	XP_016860308.1:p.Tyr31115Ter
XM_017004820.1:c.88743T>G (TTN)	XP_016860309.1:p.Tyr29581Ter
XM_017004821.1:c.88740T>G (TTN)	XP_016860310.1:p.Tyr29580Ter
XM_017004822.1:c.85782T>G (TTN)	XP_016860311.1:p.Tyr28594Ter
XM_017004823.1:c.67398T>G (TTN)	XP_016860312.1:p.Tyr22466Ter
XM_024453094.1:c.88893T>G (TTN)	XP_024308862.1:p.Tyr29631Ter
XM_024453095.1:c.88890T>G (TTN)	XP_024308863.1:p.Tyr29630Ter
XM_024453096.1:c.88323T>G (TTN)	XP_024308864.1:p.Tyr29441Ter
XM_024453097.1:c.85665T>G (TTN)	XP_024308865.1:p.Tyr28555Ter
XM_024453098.1:c.85584T>G (TTN)	XP_024308866.1:p.Tyr28528Ter
XM_024453099.1:c.67347T>G (TTN)	XP_024308867.1:p.Tyr22449Ter
XM_024453100.1:c.57201T>G (TTN)	XP_024308868.1:p.Tyr19067Ter