Canonical Allele Identifier: CA1310537691

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586706C= , CM000664.2:g.178586706C=	GRCh38
NC_000002.11:g.179451433C= , CM000664.1:g.179451433C=	GRCh37
NC_000002.10:g.179159679C=	NCBI36
NG_011618.3:g.249097G= , LRG_391:g.249097G=
NG_051363.1:g.68880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.56491G= (TTN)	ENSP00000343764.6:p.Asp18831=
ENST00000342175.11:c.37576G= (TTN)	ENSP00000340554.6:p.Asp12526=
ENST00000359218.10:c.37375G= (TTN)	ENSP00000352154.5:p.Asp12459=
ENST00000342175.10:c.37576G= (TTN)	ENSP00000340554.6:p.Asp12526=
ENST00000342992.10:c.56491G= (TTN)	ENSP00000343764.6:p.Asp18831=
ENST00000359218.9:c.37375G= (TTN)	ENSP00000352154.5:p.Asp12459=
ENST00000460472.6:c.37000G= (TTN)	ENSP00000434586.1:p.Asp12334=
ENST00000589042.5:c.64195G= (TTN) MANE Select	ENSP00000467141.1:p.Asp21399=
ENST00000591111.5:c.59272G= (TTN)	ENSP00000465570.1:p.Asp19758=
ENST00000615779.4:c.59272G= (TTN)	ENSP00000483597.1:p.Asp19758=
NM_001256850.1:c.59272G= (TTN)	NP_001243779.1:p.Asp19758=
NM_001267550.2:c.64195G= (TTN) MANE Select	NP_001254479.2:p.Asp21399=
NM_003319.4:c.37000G= (TTN)	NP_003310.4:p.Asp12334=
NM_133378.4:c.56491G= (TTN)	NP_596869.4:p.Asp18831=
NM_133432.3:c.37375G= (TTN)	NP_597676.3:p.Asp12459=
NM_133437.4:c.37576G= (TTN)	NP_597681.4:p.Asp12526=
NR_038271.1:n.597-10890C= (TTN-AS1)
NR_038272.1:n.3188+1713C= (TTN-AS1)
XM_011511729.1:c.63292G= (TTN)	XP_011510031.1:p.Asp21098=
XM_011511730.1:c.37186G= (TTN)	XP_011510032.1:p.Asp12396=
XM_011511731.1:c.37045G= (TTN)	XP_011510033.1:p.Asp12349=
XM_017004819.1:c.63088G= (TTN)	XP_016860308.1:p.Asp21030=
XM_017004820.1:c.58486G= (TTN)	XP_016860309.1:p.Asp19496=
XM_017004821.1:c.58483G= (TTN)	XP_016860310.1:p.Asp19495=
XM_017004822.1:c.55525G= (TTN)	XP_016860311.1:p.Asp18509=
XM_017004823.1:c.37141G= (TTN)	XP_016860312.1:p.Asp12381=
XM_024453094.1:c.58636G= (TTN)	XP_024308862.1:p.Asp19546=
XM_024453095.1:c.58633G= (TTN)	XP_024308863.1:p.Asp19545=
XM_024453096.1:c.58066G= (TTN)	XP_024308864.1:p.Asp19356=
XM_024453097.1:c.55408G= (TTN)	XP_024308865.1:p.Asp18470=
XM_024453098.1:c.55327G= (TTN)	XP_024308866.1:p.Asp18443=
XM_024453099.1:c.37090G= (TTN)	XP_024308867.1:p.Asp12364=
XM_024453100.1:c.26944G= (TTN)	XP_024308868.1:p.Asp8982=