Canonical Allele Identifier: CA349480076

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179455742T>A (hg19) ; chr2:g.178591015T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591015T>A , CM000664.2:g.178591015T>A	GRCh38
NC_000002.11:g.179455742T>A , CM000664.1:g.179455742T>A	GRCh37
NC_000002.10:g.179163988T>A	NCBI36
NG_011618.3:g.244788A>T , LRG_391:g.244788A>T
NG_051363.1:g.73189T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.53006A>T (TTN)	ENSP00000343764.6:p.Gln17669Leu
ENST00000342175.11:c.34091A>T (TTN)	ENSP00000340554.6:p.Gln11364Leu
ENST00000359218.10:c.33890A>T (TTN)	ENSP00000352154.5:p.Gln11297Leu
ENST00000342175.10:c.34091A>T (TTN)	ENSP00000340554.6:p.Gln11364Leu
ENST00000342992.10:c.53006A>T (TTN)	ENSP00000343764.6:p.Gln17669Leu
ENST00000359218.9:c.33890A>T (TTN)	ENSP00000352154.5:p.Gln11297Leu
ENST00000460472.6:c.33515A>T (TTN)	ENSP00000434586.1:p.Gln11172Leu
ENST00000589042.5:c.60710A>T (TTN) MANE Select	ENSP00000467141.1:p.Gln20237Leu
ENST00000591111.5:c.55787A>T (TTN)	ENSP00000465570.1:p.Gln18596Leu
ENST00000615779.4:c.55787A>T (TTN)	ENSP00000483597.1:p.Gln18596Leu
NM_001256850.1:c.55787A>T (TTN)	NP_001243779.1:p.Gln18596Leu
NM_001267550.2:c.60710A>T (TTN) MANE Select	NP_001254479.2:p.Gln20237Leu
NM_003319.4:c.33515A>T (TTN)	NP_003310.4:p.Gln11172Leu
NM_133378.4:c.53006A>T (TTN)	NP_596869.4:p.Gln17669Leu
NM_133432.3:c.33890A>T (TTN)	NP_597676.3:p.Gln11297Leu
NM_133437.4:c.34091A>T (TTN)	NP_597681.4:p.Gln11364Leu
NR_038271.1:n.597-6581T>A (TTN-AS1)
NR_038272.1:n.3189-124T>A (TTN-AS1)
XM_011511729.1:c.59807A>T (TTN)	XP_011510031.1:p.Gln19936Leu
XM_011511730.1:c.33701A>T (TTN)	XP_011510032.1:p.Gln11234Leu
XM_011511731.1:c.33560A>T (TTN)	XP_011510033.1:p.Gln11187Leu
XM_017004819.1:c.59603A>T (TTN)	XP_016860308.1:p.Gln19868Leu
XM_017004820.1:c.55001A>T (TTN)	XP_016860309.1:p.Gln18334Leu
XM_017004821.1:c.54998A>T (TTN)	XP_016860310.1:p.Gln18333Leu
XM_017004822.1:c.52040A>T (TTN)	XP_016860311.1:p.Gln17347Leu
XM_017004823.1:c.33656A>T (TTN)	XP_016860312.1:p.Gln11219Leu
XM_024453094.1:c.55151A>T (TTN)	XP_024308862.1:p.Gln18384Leu
XM_024453095.1:c.55148A>T (TTN)	XP_024308863.1:p.Gln18383Leu
XM_024453096.1:c.54581A>T (TTN)	XP_024308864.1:p.Gln18194Leu
XM_024453097.1:c.51923A>T (TTN)	XP_024308865.1:p.Gln17308Leu
XM_024453098.1:c.51842A>T (TTN)	XP_024308866.1:p.Gln17281Leu
XM_024453099.1:c.33605A>T (TTN)	XP_024308867.1:p.Gln11202Leu
XM_024453100.1:c.23459A>T (TTN)	XP_024308868.1:p.Gln7820Leu