Canonical Allele Identifier: CA430105645

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178615462A>G , CM000664.2:g.178615462A>G	GRCh38
NC_000002.11:g.179480189A>G , CM000664.1:g.179480189A>G	GRCh37
NC_000002.10:g.179188434A>G	NCBI36
NG_011618.3:g.220341T>C , LRG_391:g.220341T>C
NG_051363.1:g.97636A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.48483T>C (TTN) MANE Select	NP_001254479.2:p.Asn16161=
ENST00000589042.5:c.48483T>C (TTN) MANE Select	ENSP00000467141.1:p.Asn16161=
NM_001256850.1:c.43560T>C (TTN)	NP_001243779.1:p.Asn14520=
NM_003319.4:c.21288T>C (TTN)	NP_003310.4:p.Asn7096=
NM_133378.4:c.40779T>C (TTN)	NP_596869.4:p.Asn13593=
NM_133432.3:c.21663T>C (TTN)	NP_597676.3:p.Asn7221=
NM_133437.4:c.21864T>C (TTN)	NP_597681.4:p.Asn7288=
NR_038271.1:n.1604+88A>G (TTN-AS1)
ENST00000342175.10:c.21864T>C (TTN)	ENSP00000340554.6:p.Asn7288=
ENST00000342175.11:c.21864T>C (TTN)	ENSP00000340554.6:p.Asn7288=
ENST00000342992.10:c.40779T>C (TTN)	ENSP00000343764.6:p.Asn13593=
ENST00000342992.11:c.40779T>C (TTN)	ENSP00000343764.6:p.Asn13593=
ENST00000359218.10:c.21663T>C (TTN)	ENSP00000352154.5:p.Asn7221=
ENST00000359218.9:c.21663T>C (TTN)	ENSP00000352154.5:p.Asn7221=
ENST00000460472.6:c.21288T>C (TTN)	ENSP00000434586.1:p.Asn7096=
ENST00000591111.5:c.43560T>C (TTN)	ENSP00000465570.1:p.Asn14520=
ENST00000615779.4:c.43560T>C (TTN)	ENSP00000483597.1:p.Asn14520=
XM_011511729.1:c.47580T>C (TTN)	XP_011510031.1:p.Asn15860=
XM_011511730.1:c.21474T>C (TTN)	XP_011510032.1:p.Asn7158=
XM_011511731.1:c.21333T>C (TTN)	XP_011510033.1:p.Asn7111=
XM_017004819.1:c.47376T>C (TTN)	XP_016860308.1:p.Asn15792=
XM_017004820.1:c.42774T>C (TTN)	XP_016860309.1:p.Asn14258=
XM_017004821.1:c.42771T>C (TTN)	XP_016860310.1:p.Asn14257=
XM_017004822.1:c.39813T>C (TTN)	XP_016860311.1:p.Asn13271=
XM_017004823.1:c.21429T>C (TTN)	XP_016860312.1:p.Asn7143=
XM_024453094.1:c.42924T>C (TTN)	XP_024308862.1:p.Asn14308=
XM_024453095.1:c.42921T>C (TTN)	XP_024308863.1:p.Asn14307=
XM_024453096.1:c.42354T>C (TTN)	XP_024308864.1:p.Asn14118=
XM_024453097.1:c.39696T>C (TTN)	XP_024308865.1:p.Asn13232=
XM_024453098.1:c.39615T>C (TTN)	XP_024308866.1:p.Asn13205=
XM_024453099.1:c.21378T>C (TTN)	XP_024308867.1:p.Asn7126=
XM_024453100.1:c.11232T>C (TTN)	XP_024308868.1:p.Asn3744=