Canonical Allele Identifier: CA1310521544

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544363A= , CM000664.2:g.178544363A=	GRCh38
NC_000002.11:g.179409090A= , CM000664.1:g.179409090A=	GRCh37
NC_000002.10:g.179117336A=	NCBI36
NG_011618.3:g.291440T= , LRG_391:g.291440T=
NG_051363.1:g.26537A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88162T= (TTN)	ENSP00000343764.6:p.Trp29388=
ENST00000342175.11:c.69247T= (TTN)	ENSP00000340554.6:p.Trp23083=
ENST00000359218.10:c.69046T= (TTN)	ENSP00000352154.5:p.Trp23016=
ENST00000342175.10:c.69247T= (TTN)	ENSP00000340554.6:p.Trp23083=
ENST00000342992.10:c.88162T= (TTN)	ENSP00000343764.6:p.Trp29388=
ENST00000359218.9:c.69046T= (TTN)	ENSP00000352154.5:p.Trp23016=
ENST00000460472.6:c.68671T= (TTN)	ENSP00000434586.1:p.Trp22891=
ENST00000589042.5:c.95866T= (TTN) MANE Select	ENSP00000467141.1:p.Trp31956=
ENST00000591111.5:c.90943T= (TTN)	ENSP00000465570.1:p.Trp30315=
ENST00000615779.4:c.90943T= (TTN)	ENSP00000483597.1:p.Trp30315=
NM_001256850.1:c.90943T= (TTN)	NP_001243779.1:p.Trp30315=
NM_001267550.2:c.95866T= (TTN) MANE Select	NP_001254479.2:p.Trp31956=
NM_003319.4:c.68671T= (TTN)	NP_003310.4:p.Trp22891=
NM_133378.4:c.88162T= (TTN)	NP_596869.4:p.Trp29388=
NM_133432.3:c.69046T= (TTN)	NP_597676.3:p.Trp23016=
NM_133437.4:c.69247T= (TTN)	NP_597681.4:p.Trp23083=
NR_038271.1:n.446+20727A= (TTN-AS1)
NR_038272.1:n.2043+2002A= (TTN-AS1)
XM_011511729.1:c.94963T= (TTN)	XP_011510031.1:p.Trp31655=
XM_011511730.1:c.68857T= (TTN)	XP_011510032.1:p.Trp22953=
XM_011511731.1:c.68716T= (TTN)	XP_011510033.1:p.Trp22906=
XM_017004819.1:c.94759T= (TTN)	XP_016860308.1:p.Trp31587=
XM_017004820.1:c.90157T= (TTN)	XP_016860309.1:p.Trp30053=
XM_017004821.1:c.90154T= (TTN)	XP_016860310.1:p.Trp30052=
XM_017004822.1:c.87196T= (TTN)	XP_016860311.1:p.Trp29066=
XM_017004823.1:c.68812T= (TTN)	XP_016860312.1:p.Trp22938=
XM_024453094.1:c.90307T= (TTN)	XP_024308862.1:p.Trp30103=
XM_024453095.1:c.90304T= (TTN)	XP_024308863.1:p.Trp30102=
XM_024453096.1:c.89737T= (TTN)	XP_024308864.1:p.Trp29913=
XM_024453097.1:c.87079T= (TTN)	XP_024308865.1:p.Trp29027=
XM_024453098.1:c.86998T= (TTN)	XP_024308866.1:p.Trp29000=
XM_024453099.1:c.68761T= (TTN)	XP_024308867.1:p.Trp22921=
XM_024453100.1:c.58615T= (TTN)	XP_024308868.1:p.Trp19539=