Canonical Allele Identifier: CA1310527724

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178562091G= , CM000664.2:g.178562091G=	GRCh38
NC_000002.11:g.179426818G= , CM000664.1:g.179426818G=	GRCh37
NC_000002.10:g.179135064G=	NCBI36
NG_011618.3:g.273712C= , LRG_391:g.273712C=
NG_051363.1:g.44265G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.76337C= (TTN)	ENSP00000343764.6:p.Ser25446=
ENST00000342175.11:c.57422C= (TTN)	ENSP00000340554.6:p.Ser19141=
ENST00000359218.10:c.57221C= (TTN)	ENSP00000352154.5:p.Ser19074=
ENST00000342175.10:c.57422C= (TTN)	ENSP00000340554.6:p.Ser19141=
ENST00000342992.10:c.76337C= (TTN)	ENSP00000343764.6:p.Ser25446=
ENST00000359218.9:c.57221C= (TTN)	ENSP00000352154.5:p.Ser19074=
ENST00000460472.6:c.56846C= (TTN)	ENSP00000434586.1:p.Ser18949=
ENST00000589042.5:c.84041C= (TTN) MANE Select	ENSP00000467141.1:p.Ser28014=
ENST00000591111.5:c.79118C= (TTN)	ENSP00000465570.1:p.Ser26373=
ENST00000615779.4:c.79118C= (TTN)	ENSP00000483597.1:p.Ser26373=
NM_001256850.1:c.79118C= (TTN)	NP_001243779.1:p.Ser26373=
NM_001267550.2:c.84041C= (TTN) MANE Select	NP_001254479.2:p.Ser28014=
NM_003319.4:c.56846C= (TTN)	NP_003310.4:p.Ser18949=
NM_133378.4:c.76337C= (TTN)	NP_596869.4:p.Ser25446=
NM_133432.3:c.57221C= (TTN)	NP_597676.3:p.Ser19074=
NM_133437.4:c.57422C= (TTN)	NP_597681.4:p.Ser19141=
NR_038271.1:n.447-9209G= (TTN-AS1)
NR_038272.1:n.2043+19730G= (TTN-AS1)
XM_011511729.1:c.83138C= (TTN)	XP_011510031.1:p.Ser27713=
XM_011511730.1:c.57032C= (TTN)	XP_011510032.1:p.Ser19011=
XM_011511731.1:c.56891C= (TTN)	XP_011510033.1:p.Ser18964=
XM_017004819.1:c.82934C= (TTN)	XP_016860308.1:p.Ser27645=
XM_017004820.1:c.78332C= (TTN)	XP_016860309.1:p.Ser26111=
XM_017004821.1:c.78329C= (TTN)	XP_016860310.1:p.Ser26110=
XM_017004822.1:c.75371C= (TTN)	XP_016860311.1:p.Ser25124=
XM_017004823.1:c.56987C= (TTN)	XP_016860312.1:p.Ser18996=
XM_024453094.1:c.78482C= (TTN)	XP_024308862.1:p.Ser26161=
XM_024453095.1:c.78479C= (TTN)	XP_024308863.1:p.Ser26160=
XM_024453096.1:c.77912C= (TTN)	XP_024308864.1:p.Ser25971=
XM_024453097.1:c.75254C= (TTN)	XP_024308865.1:p.Ser25085=
XM_024453098.1:c.75173C= (TTN)	XP_024308866.1:p.Ser25058=
XM_024453099.1:c.56936C= (TTN)	XP_024308867.1:p.Ser18979=
XM_024453100.1:c.46790C= (TTN)	XP_024308868.1:p.Ser15597=