Canonical Allele Identifier: CA349401258

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178528300G>C , CM000664.2:g.178528300G>C	GRCh38
NC_000002.11:g.179393027G>C , CM000664.1:g.179393027G>C	GRCh37
NC_000002.10:g.179101273G>C	NCBI36
NG_011618.3:g.307503C>G , LRG_391:g.307503C>G
NG_051363.1:g.10474G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107351C>G (TTN) MANE Select	NP_001254479.2:p.Ser35784Ter
ENST00000589042.5:c.107351C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser35784Ter
NM_001256850.1:c.102428C>G (TTN)	NP_001243779.1:p.Ser34143Ter
NM_003319.4:c.80156C>G (TTN)	NP_003310.4:p.Ser26719Ter
NM_133378.4:c.99647C>G (TTN)	NP_596869.4:p.Ser33216Ter
NM_133432.3:c.80531C>G (TTN)	NP_597676.3:p.Ser26844Ter
NM_133437.4:c.80732C>G (TTN)	NP_597681.4:p.Ser26911Ter
NR_038271.1:n.446+4664G>C (TTN-AS1)
NR_038272.1:n.219+4664G>C (TTN-AS1)
ENST00000342175.10:c.80732C>G (TTN)	ENSP00000340554.6:p.Ser26911Ter
ENST00000342175.11:c.80732C>G (TTN)	ENSP00000340554.6:p.Ser26911Ter
ENST00000342992.10:c.99647C>G (TTN)	ENSP00000343764.6:p.Ser33216Ter
ENST00000342992.11:c.99647C>G (TTN)	ENSP00000343764.6:p.Ser33216Ter
ENST00000359218.10:c.80531C>G (TTN)	ENSP00000352154.5:p.Ser26844Ter
ENST00000359218.9:c.80531C>G (TTN)	ENSP00000352154.5:p.Ser26844Ter
ENST00000460472.6:c.80156C>G (TTN)	ENSP00000434586.1:p.Ser26719Ter
ENST00000591111.5:c.102428C>G (TTN)	ENSP00000465570.1:p.Ser34143Ter
ENST00000615779.4:c.102428C>G (TTN)	ENSP00000483597.1:p.Ser34143Ter
XM_011511729.1:c.106448C>G (TTN)	XP_011510031.1:p.Ser35483Ter
XM_011511730.1:c.80342C>G (TTN)	XP_011510032.1:p.Ser26781Ter
XM_011511731.1:c.80201C>G (TTN)	XP_011510033.1:p.Ser26734Ter
XM_017004819.1:c.106244C>G (TTN)	XP_016860308.1:p.Ser35415Ter
XM_017004820.1:c.101642C>G (TTN)	XP_016860309.1:p.Ser33881Ter
XM_017004821.1:c.101639C>G (TTN)	XP_016860310.1:p.Ser33880Ter
XM_017004822.1:c.98681C>G (TTN)	XP_016860311.1:p.Ser32894Ter
XM_017004823.1:c.80297C>G (TTN)	XP_016860312.1:p.Ser26766Ter
XM_024453094.1:c.101792C>G (TTN)	XP_024308862.1:p.Ser33931Ter
XM_024453095.1:c.101789C>G (TTN)	XP_024308863.1:p.Ser33930Ter
XM_024453096.1:c.101222C>G (TTN)	XP_024308864.1:p.Ser33741Ter
XM_024453097.1:c.98564C>G (TTN)	XP_024308865.1:p.Ser32855Ter
XM_024453098.1:c.98483C>G (TTN)	XP_024308866.1:p.Ser32828Ter
XM_024453099.1:c.80246C>G (TTN)	XP_024308867.1:p.Ser26749Ter
XM_024453100.1:c.70100C>G (TTN)	XP_024308868.1:p.Ser23367Ter