Canonical Allele Identifier: CA349425756

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178580533A>C , CM000664.2:g.178580533A>C	GRCh38
NC_000002.11:g.179445260A>C , CM000664.1:g.179445260A>C	GRCh37
NC_000002.10:g.179153506A>C	NCBI36
NG_011618.3:g.255270T>G , LRG_391:g.255270T>G
NG_051363.1:g.62707A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66846T>G (TTN) MANE Select	NP_001254479.2:p.Tyr22282Ter
ENST00000589042.5:c.66846T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr22282Ter
NM_001256850.1:c.61923T>G (TTN)	NP_001243779.1:p.Tyr20641Ter
NM_003319.4:c.39651T>G (TTN)	NP_003310.4:p.Tyr13217Ter
NM_133378.4:c.59142T>G (TTN)	NP_596869.4:p.Tyr19714Ter
NM_133432.3:c.40026T>G (TTN)	NP_597676.3:p.Tyr13342Ter
NM_133437.4:c.40227T>G (TTN)	NP_597681.4:p.Tyr13409Ter
NR_038271.1:n.596+9084A>C (TTN-AS1)
NR_038272.1:n.2044-2039A>C (TTN-AS1)
ENST00000342175.10:c.40227T>G (TTN)	ENSP00000340554.6:p.Tyr13409Ter
ENST00000342175.11:c.40227T>G (TTN)	ENSP00000340554.6:p.Tyr13409Ter
ENST00000342992.10:c.59142T>G (TTN)	ENSP00000343764.6:p.Tyr19714Ter
ENST00000342992.11:c.59142T>G (TTN)	ENSP00000343764.6:p.Tyr19714Ter
ENST00000359218.10:c.40026T>G (TTN)	ENSP00000352154.5:p.Tyr13342Ter
ENST00000359218.9:c.40026T>G (TTN)	ENSP00000352154.5:p.Tyr13342Ter
ENST00000460472.6:c.39651T>G (TTN)	ENSP00000434586.1:p.Tyr13217Ter
ENST00000591111.5:c.61923T>G (TTN)	ENSP00000465570.1:p.Tyr20641Ter
ENST00000615779.4:c.61923T>G (TTN)	ENSP00000483597.1:p.Tyr20641Ter
XM_011511729.1:c.65943T>G (TTN)	XP_011510031.1:p.Tyr21981Ter
XM_011511730.1:c.39837T>G (TTN)	XP_011510032.1:p.Tyr13279Ter
XM_011511731.1:c.39696T>G (TTN)	XP_011510033.1:p.Tyr13232Ter
XM_017004819.1:c.65739T>G (TTN)	XP_016860308.1:p.Tyr21913Ter
XM_017004820.1:c.61137T>G (TTN)	XP_016860309.1:p.Tyr20379Ter
XM_017004821.1:c.61134T>G (TTN)	XP_016860310.1:p.Tyr20378Ter
XM_017004822.1:c.58176T>G (TTN)	XP_016860311.1:p.Tyr19392Ter
XM_017004823.1:c.39792T>G (TTN)	XP_016860312.1:p.Tyr13264Ter
XM_024453094.1:c.61287T>G (TTN)	XP_024308862.1:p.Tyr20429Ter
XM_024453095.1:c.61284T>G (TTN)	XP_024308863.1:p.Tyr20428Ter
XM_024453096.1:c.60717T>G (TTN)	XP_024308864.1:p.Tyr20239Ter
XM_024453097.1:c.58059T>G (TTN)	XP_024308865.1:p.Tyr19353Ter
XM_024453098.1:c.57978T>G (TTN)	XP_024308866.1:p.Tyr19326Ter
XM_024453099.1:c.39741T>G (TTN)	XP_024308867.1:p.Tyr13247Ter
XM_024453100.1:c.29595T>G (TTN)	XP_024308868.1:p.Tyr9865Ter