Canonical Allele Identifier: CA1310549416

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614551A= , CM000664.2:g.178614551A=	GRCh38
NC_000002.11:g.179479278A= , CM000664.1:g.179479278A=	GRCh37
NC_000002.10:g.179187523A=	NCBI36
NG_011618.3:g.221252T= , LRG_391:g.221252T=
NG_051363.1:g.96725A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41259T= (TTN)	ENSP00000343764.6:p.Ser13753=
ENST00000342175.11:c.22344T= (TTN)	ENSP00000340554.6:p.Ser7448=
ENST00000359218.10:c.22143T= (TTN)	ENSP00000352154.5:p.Ser7381=
ENST00000342175.10:c.22344T= (TTN)	ENSP00000340554.6:p.Ser7448=
ENST00000342992.10:c.41259T= (TTN)	ENSP00000343764.6:p.Ser13753=
ENST00000359218.9:c.22143T= (TTN)	ENSP00000352154.5:p.Ser7381=
ENST00000460472.6:c.21768T= (TTN)	ENSP00000434586.1:p.Ser7256=
ENST00000589042.5:c.48963T= (TTN) MANE Select	ENSP00000467141.1:p.Ser16321=
ENST00000591111.5:c.44040T= (TTN)	ENSP00000465570.1:p.Ser14680=
ENST00000615779.4:c.44040T= (TTN)	ENSP00000483597.1:p.Ser14680=
NM_001256850.1:c.44040T= (TTN)	NP_001243779.1:p.Ser14680=
NM_001267550.2:c.48963T= (TTN) MANE Select	NP_001254479.2:p.Ser16321=
NM_003319.4:c.21768T= (TTN)	NP_003310.4:p.Ser7256=
NM_133378.4:c.41259T= (TTN)	NP_596869.4:p.Ser13753=
NM_133432.3:c.22143T= (TTN)	NP_597676.3:p.Ser7381=
NM_133437.4:c.22344T= (TTN)	NP_597681.4:p.Ser7448=
NR_038271.1:n.1299A= (TTN-AS1)
XM_011511729.1:c.48060T= (TTN)	XP_011510031.1:p.Ser16020=
XM_011511730.1:c.21954T= (TTN)	XP_011510032.1:p.Ser7318=
XM_011511731.1:c.21813T= (TTN)	XP_011510033.1:p.Ser7271=
XM_017004819.1:c.47856T= (TTN)	XP_016860308.1:p.Ser15952=
XM_017004820.1:c.43254T= (TTN)	XP_016860309.1:p.Ser14418=
XM_017004821.1:c.43251T= (TTN)	XP_016860310.1:p.Ser14417=
XM_017004822.1:c.40293T= (TTN)	XP_016860311.1:p.Ser13431=
XM_017004823.1:c.21909T= (TTN)	XP_016860312.1:p.Ser7303=
XM_024453094.1:c.43404T= (TTN)	XP_024308862.1:p.Ser14468=
XM_024453095.1:c.43401T= (TTN)	XP_024308863.1:p.Ser14467=
XM_024453096.1:c.42834T= (TTN)	XP_024308864.1:p.Ser14278=
XM_024453097.1:c.40176T= (TTN)	XP_024308865.1:p.Ser13392=
XM_024453098.1:c.40095T= (TTN)	XP_024308866.1:p.Ser13365=
XM_024453099.1:c.21858T= (TTN)	XP_024308867.1:p.Ser7286=
XM_024453100.1:c.11712T= (TTN)	XP_024308868.1:p.Ser3904=