Canonical Allele Identifier: CA349411775

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396923T>C (hg19) ; chr2:g.178532196T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532196T>C , CM000664.2:g.178532196T>C	GRCh38
NC_000002.11:g.179396923T>C , CM000664.1:g.179396923T>C	GRCh37
NC_000002.10:g.179105169T>C	NCBI36
NG_011618.3:g.303607A>G , LRG_391:g.303607A>G
NG_051363.1:g.14370T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96715A>G (TTN)	ENSP00000343764.6:p.Arg32239Gly
ENST00000342175.11:c.77800A>G (TTN)	ENSP00000340554.6:p.Arg25934Gly
ENST00000359218.10:c.77599A>G (TTN)	ENSP00000352154.5:p.Arg25867Gly
ENST00000342175.10:c.77800A>G (TTN)	ENSP00000340554.6:p.Arg25934Gly
ENST00000342992.10:c.96715A>G (TTN)	ENSP00000343764.6:p.Arg32239Gly
ENST00000359218.9:c.77599A>G (TTN)	ENSP00000352154.5:p.Arg25867Gly
ENST00000460472.6:c.77224A>G (TTN)	ENSP00000434586.1:p.Arg25742Gly
ENST00000589042.5:c.104419A>G (TTN) MANE Select	ENSP00000467141.1:p.Arg34807Gly
ENST00000591111.5:c.99496A>G (TTN)	ENSP00000465570.1:p.Arg33166Gly
ENST00000615779.4:c.99496A>G (TTN)	ENSP00000483597.1:p.Arg33166Gly
NM_001256850.1:c.99496A>G (TTN)	NP_001243779.1:p.Arg33166Gly
NM_001267550.2:c.104419A>G (TTN) MANE Select	NP_001254479.2:p.Arg34807Gly
NM_003319.4:c.77224A>G (TTN)	NP_003310.4:p.Arg25742Gly
NM_133378.4:c.96715A>G (TTN)	NP_596869.4:p.Arg32239Gly
NM_133432.3:c.77599A>G (TTN)	NP_597676.3:p.Arg25867Gly
NM_133437.4:c.77800A>G (TTN)	NP_597681.4:p.Arg25934Gly
NR_038271.1:n.446+8560T>C (TTN-AS1)
NR_038272.1:n.220-3536T>C (TTN-AS1)
XM_011511729.1:c.103516A>G (TTN)	XP_011510031.1:p.Arg34506Gly
XM_011511730.1:c.77410A>G (TTN)	XP_011510032.1:p.Arg25804Gly
XM_011511731.1:c.77269A>G (TTN)	XP_011510033.1:p.Arg25757Gly
XM_017004819.1:c.103312A>G (TTN)	XP_016860308.1:p.Arg34438Gly
XM_017004820.1:c.98710A>G (TTN)	XP_016860309.1:p.Arg32904Gly
XM_017004821.1:c.98707A>G (TTN)	XP_016860310.1:p.Arg32903Gly
XM_017004822.1:c.95749A>G (TTN)	XP_016860311.1:p.Arg31917Gly
XM_017004823.1:c.77365A>G (TTN)	XP_016860312.1:p.Arg25789Gly
XM_024453094.1:c.98860A>G (TTN)	XP_024308862.1:p.Arg32954Gly
XM_024453095.1:c.98857A>G (TTN)	XP_024308863.1:p.Arg32953Gly
XM_024453096.1:c.98290A>G (TTN)	XP_024308864.1:p.Arg32764Gly
XM_024453097.1:c.95632A>G (TTN)	XP_024308865.1:p.Arg31878Gly
XM_024453098.1:c.95551A>G (TTN)	XP_024308866.1:p.Arg31851Gly
XM_024453099.1:c.77314A>G (TTN)	XP_024308867.1:p.Arg25772Gly
XM_024453100.1:c.67168A>G (TTN)	XP_024308868.1:p.Arg22390Gly