Canonical Allele Identifier: CA10576455

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178542323T>G , CM000664.2:g.178542323T>G	GRCh38
NC_000002.11:g.179407050T>G , CM000664.1:g.179407050T>G	GRCh37
NC_000002.10:g.179115296T>G	NCBI36
NG_011618.3:g.293480A>C , LRG_391:g.293480A>C
NG_051363.1:g.24497T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.89729A>C (TTN)	ENSP00000343764.6:p.Asn29910Thr
ENST00000342175.11:c.70814A>C (TTN)	ENSP00000340554.6:p.Asn23605Thr
ENST00000359218.10:c.70613A>C (TTN)	ENSP00000352154.5:p.Asn23538Thr
ENST00000342175.10:c.70814A>C (TTN)	ENSP00000340554.6:p.Asn23605Thr
ENST00000342992.10:c.89729A>C (TTN)	ENSP00000343764.6:p.Asn29910Thr
ENST00000359218.9:c.70613A>C (TTN)	ENSP00000352154.5:p.Asn23538Thr
ENST00000460472.6:c.70238A>C (TTN)	ENSP00000434586.1:p.Asn23413Thr
ENST00000589042.5:c.97433A>C (TTN) MANE Select	ENSP00000467141.1:p.Asn32478Thr
ENST00000591111.5:c.92510A>C (TTN)	ENSP00000465570.1:p.Asn30837Thr
ENST00000615779.4:c.92510A>C (TTN)	ENSP00000483597.1:p.Asn30837Thr
NM_001256850.1:c.92510A>C (TTN)	NP_001243779.1:p.Asn30837Thr
NM_001267550.2:c.97433A>C (TTN) MANE Select	NP_001254479.2:p.Asn32478Thr
NM_003319.4:c.70238A>C (TTN)	NP_003310.4:p.Asn23413Thr
NM_133378.4:c.89729A>C (TTN)	NP_596869.4:p.Asn29910Thr
NM_133432.3:c.70613A>C (TTN)	NP_597676.3:p.Asn23538Thr
NM_133437.4:c.70814A>C (TTN)	NP_597681.4:p.Asn23605Thr
NR_038271.1:n.446+18687T>G (TTN-AS1)
NR_038272.1:n.2005T>G (TTN-AS1)
XM_011511729.1:c.96530A>C (TTN)	XP_011510031.1:p.Asn32177Thr
XM_011511730.1:c.70424A>C (TTN)	XP_011510032.1:p.Asn23475Thr
XM_011511731.1:c.70283A>C (TTN)	XP_011510033.1:p.Asn23428Thr
XM_017004819.1:c.96326A>C (TTN)	XP_016860308.1:p.Asn32109Thr
XM_017004820.1:c.91724A>C (TTN)	XP_016860309.1:p.Asn30575Thr
XM_017004821.1:c.91721A>C (TTN)	XP_016860310.1:p.Asn30574Thr
XM_017004822.1:c.88763A>C (TTN)	XP_016860311.1:p.Asn29588Thr
XM_017004823.1:c.70379A>C (TTN)	XP_016860312.1:p.Asn23460Thr
XM_024453094.1:c.91874A>C (TTN)	XP_024308862.1:p.Asn30625Thr
XM_024453095.1:c.91871A>C (TTN)	XP_024308863.1:p.Asn30624Thr
XM_024453096.1:c.91304A>C (TTN)	XP_024308864.1:p.Asn30435Thr
XM_024453097.1:c.88646A>C (TTN)	XP_024308865.1:p.Asn29549Thr
XM_024453098.1:c.88565A>C (TTN)	XP_024308866.1:p.Asn29522Thr
XM_024453099.1:c.70328A>C (TTN)	XP_024308867.1:p.Asn23443Thr
XM_024453100.1:c.60182A>C (TTN)	XP_024308868.1:p.Asn20061Thr