Canonical Allele Identifier: CA349542199

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178559456C>T , CM000664.2:g.178559456C>T	GRCh38
NC_000002.11:g.179424183C>T , CM000664.1:g.179424183C>T	GRCh37
NC_000002.10:g.179132429C>T	NCBI36
NG_011618.3:g.276347G>A , LRG_391:g.276347G>A
NG_051363.1:g.41630C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.86676G>A (TTN) MANE Select	NP_001254479.2:p.Trp28892Ter
ENST00000589042.5:c.86676G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp28892Ter
NM_001256850.1:c.81753G>A (TTN)	NP_001243779.1:p.Trp27251Ter
NM_003319.4:c.59481G>A (TTN)	NP_003310.4:p.Trp19827Ter
NM_133378.4:c.78972G>A (TTN)	NP_596869.4:p.Trp26324Ter
NM_133432.3:c.59856G>A (TTN)	NP_597676.3:p.Trp19952Ter
NM_133437.4:c.60057G>A (TTN)	NP_597681.4:p.Trp20019Ter
NR_038271.1:n.447-11844C>T (TTN-AS1)
NR_038272.1:n.2043+17095C>T (TTN-AS1)
ENST00000342175.10:c.60057G>A (TTN)	ENSP00000340554.6:p.Trp20019Ter
ENST00000342175.11:c.60057G>A (TTN)	ENSP00000340554.6:p.Trp20019Ter
ENST00000342992.10:c.78972G>A (TTN)	ENSP00000343764.6:p.Trp26324Ter
ENST00000342992.11:c.78972G>A (TTN)	ENSP00000343764.6:p.Trp26324Ter
ENST00000359218.10:c.59856G>A (TTN)	ENSP00000352154.5:p.Trp19952Ter
ENST00000359218.9:c.59856G>A (TTN)	ENSP00000352154.5:p.Trp19952Ter
ENST00000460472.6:c.59481G>A (TTN)	ENSP00000434586.1:p.Trp19827Ter
ENST00000591111.5:c.81753G>A (TTN)	ENSP00000465570.1:p.Trp27251Ter
ENST00000615779.4:c.81753G>A (TTN)	ENSP00000483597.1:p.Trp27251Ter
XM_011511729.1:c.85773G>A (TTN)	XP_011510031.1:p.Trp28591Ter
XM_011511730.1:c.59667G>A (TTN)	XP_011510032.1:p.Trp19889Ter
XM_011511731.1:c.59526G>A (TTN)	XP_011510033.1:p.Trp19842Ter
XM_017004819.1:c.85569G>A (TTN)	XP_016860308.1:p.Trp28523Ter
XM_017004820.1:c.80967G>A (TTN)	XP_016860309.1:p.Trp26989Ter
XM_017004821.1:c.80964G>A (TTN)	XP_016860310.1:p.Trp26988Ter
XM_017004822.1:c.78006G>A (TTN)	XP_016860311.1:p.Trp26002Ter
XM_017004823.1:c.59622G>A (TTN)	XP_016860312.1:p.Trp19874Ter
XM_024453094.1:c.81117G>A (TTN)	XP_024308862.1:p.Trp27039Ter
XM_024453095.1:c.81114G>A (TTN)	XP_024308863.1:p.Trp27038Ter
XM_024453096.1:c.80547G>A (TTN)	XP_024308864.1:p.Trp26849Ter
XM_024453097.1:c.77889G>A (TTN)	XP_024308865.1:p.Trp25963Ter
XM_024453098.1:c.77808G>A (TTN)	XP_024308866.1:p.Trp25936Ter
XM_024453099.1:c.59571G>A (TTN)	XP_024308867.1:p.Trp19857Ter
XM_024453100.1:c.49425G>A (TTN)	XP_024308868.1:p.Trp16475Ter