Canonical Allele Identifier: CA349413879

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532995A>C , CM000664.2:g.178532995A>C	GRCh38
NC_000002.11:g.179397722A>C , CM000664.1:g.179397722A>C	GRCh37
NC_000002.10:g.179105968A>C	NCBI36
NG_011618.3:g.302808T>G , LRG_391:g.302808T>G
NG_051363.1:g.15169A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.103620T>G (TTN) MANE Select	NP_001254479.2:p.Tyr34540Ter
ENST00000589042.5:c.103620T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr34540Ter
NM_001256850.1:c.98697T>G (TTN)	NP_001243779.1:p.Tyr32899Ter
NM_003319.4:c.76425T>G (TTN)	NP_003310.4:p.Tyr25475Ter
NM_133378.4:c.95916T>G (TTN)	NP_596869.4:p.Tyr31972Ter
NM_133432.3:c.76800T>G (TTN)	NP_597676.3:p.Tyr25600Ter
NM_133437.4:c.77001T>G (TTN)	NP_597681.4:p.Tyr25667Ter
NR_038271.1:n.446+9359A>C (TTN-AS1)
NR_038272.1:n.220-2737A>C (TTN-AS1)
ENST00000342175.10:c.77001T>G (TTN)	ENSP00000340554.6:p.Tyr25667Ter
ENST00000342175.11:c.77001T>G (TTN)	ENSP00000340554.6:p.Tyr25667Ter
ENST00000342992.10:c.95916T>G (TTN)	ENSP00000343764.6:p.Tyr31972Ter
ENST00000342992.11:c.95916T>G (TTN)	ENSP00000343764.6:p.Tyr31972Ter
ENST00000359218.10:c.76800T>G (TTN)	ENSP00000352154.5:p.Tyr25600Ter
ENST00000359218.9:c.76800T>G (TTN)	ENSP00000352154.5:p.Tyr25600Ter
ENST00000460472.6:c.76425T>G (TTN)	ENSP00000434586.1:p.Tyr25475Ter
ENST00000591111.5:c.98697T>G (TTN)	ENSP00000465570.1:p.Tyr32899Ter
ENST00000615779.4:c.98697T>G (TTN)	ENSP00000483597.1:p.Tyr32899Ter
XM_011511729.1:c.102717T>G (TTN)	XP_011510031.1:p.Tyr34239Ter
XM_011511730.1:c.76611T>G (TTN)	XP_011510032.1:p.Tyr25537Ter
XM_011511731.1:c.76470T>G (TTN)	XP_011510033.1:p.Tyr25490Ter
XM_017004819.1:c.102513T>G (TTN)	XP_016860308.1:p.Tyr34171Ter
XM_017004820.1:c.97911T>G (TTN)	XP_016860309.1:p.Tyr32637Ter
XM_017004821.1:c.97908T>G (TTN)	XP_016860310.1:p.Tyr32636Ter
XM_017004822.1:c.94950T>G (TTN)	XP_016860311.1:p.Tyr31650Ter
XM_017004823.1:c.76566T>G (TTN)	XP_016860312.1:p.Tyr25522Ter
XM_024453094.1:c.98061T>G (TTN)	XP_024308862.1:p.Tyr32687Ter
XM_024453095.1:c.98058T>G (TTN)	XP_024308863.1:p.Tyr32686Ter
XM_024453096.1:c.97491T>G (TTN)	XP_024308864.1:p.Tyr32497Ter
XM_024453097.1:c.94833T>G (TTN)	XP_024308865.1:p.Tyr31611Ter
XM_024453098.1:c.94752T>G (TTN)	XP_024308866.1:p.Tyr31584Ter
XM_024453099.1:c.76515T>G (TTN)	XP_024308867.1:p.Tyr25505Ter
XM_024453100.1:c.66369T>G (TTN)	XP_024308868.1:p.Tyr22123Ter