Canonical Allele Identifier: CA10587459

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557447T>C , CM000664.2:g.178557447T>C	GRCh38
NC_000002.11:g.179422174T>C , CM000664.1:g.179422174T>C	GRCh37
NC_000002.10:g.179130420T>C	NCBI36
NG_011618.3:g.278356A>G , LRG_391:g.278356A>G
NG_051363.1:g.39621T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.80111A>G (TTN)	ENSP00000343764.6:p.Tyr26704Cys
ENST00000342175.11:c.61196A>G (TTN)	ENSP00000340554.6:p.Tyr20399Cys
ENST00000359218.10:c.60995A>G (TTN)	ENSP00000352154.5:p.Tyr20332Cys
ENST00000342175.10:c.61196A>G (TTN)	ENSP00000340554.6:p.Tyr20399Cys
ENST00000342992.10:c.80111A>G (TTN)	ENSP00000343764.6:p.Tyr26704Cys
ENST00000359218.9:c.60995A>G (TTN)	ENSP00000352154.5:p.Tyr20332Cys
ENST00000460472.6:c.60620A>G (TTN)	ENSP00000434586.1:p.Tyr20207Cys
ENST00000589042.5:c.87815A>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr29272Cys
ENST00000591111.5:c.82892A>G (TTN)	ENSP00000465570.1:p.Tyr27631Cys
ENST00000615779.4:c.82892A>G (TTN)	ENSP00000483597.1:p.Tyr27631Cys
NM_001256850.1:c.82892A>G (TTN)	NP_001243779.1:p.Tyr27631Cys
NM_001267550.2:c.87815A>G (TTN) MANE Select	NP_001254479.2:p.Tyr29272Cys
NM_003319.4:c.60620A>G (TTN)	NP_003310.4:p.Tyr20207Cys
NM_133378.4:c.80111A>G (TTN)	NP_596869.4:p.Tyr26704Cys
NM_133432.3:c.60995A>G (TTN)	NP_597676.3:p.Tyr20332Cys
NM_133437.4:c.61196A>G (TTN)	NP_597681.4:p.Tyr20399Cys
NR_038271.1:n.447-13853T>C (TTN-AS1)
NR_038272.1:n.2043+15086T>C (TTN-AS1)
XM_011511729.1:c.86912A>G (TTN)	XP_011510031.1:p.Tyr28971Cys
XM_011511730.1:c.60806A>G (TTN)	XP_011510032.1:p.Tyr20269Cys
XM_011511731.1:c.60665A>G (TTN)	XP_011510033.1:p.Tyr20222Cys
XM_017004819.1:c.86708A>G (TTN)	XP_016860308.1:p.Tyr28903Cys
XM_017004820.1:c.82106A>G (TTN)	XP_016860309.1:p.Tyr27369Cys
XM_017004821.1:c.82103A>G (TTN)	XP_016860310.1:p.Tyr27368Cys
XM_017004822.1:c.79145A>G (TTN)	XP_016860311.1:p.Tyr26382Cys
XM_017004823.1:c.60761A>G (TTN)	XP_016860312.1:p.Tyr20254Cys
XM_024453094.1:c.82256A>G (TTN)	XP_024308862.1:p.Tyr27419Cys
XM_024453095.1:c.82253A>G (TTN)	XP_024308863.1:p.Tyr27418Cys
XM_024453096.1:c.81686A>G (TTN)	XP_024308864.1:p.Tyr27229Cys
XM_024453097.1:c.79028A>G (TTN)	XP_024308865.1:p.Tyr26343Cys
XM_024453098.1:c.78947A>G (TTN)	XP_024308866.1:p.Tyr26316Cys
XM_024453099.1:c.60710A>G (TTN)	XP_024308867.1:p.Tyr20237Cys
XM_024453100.1:c.50564A>G (TTN)	XP_024308868.1:p.Tyr16855Cys