Canonical Allele Identifier: CA349407278

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395353C>A (hg19) ; chr2:g.178530626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530626C>A , CM000664.2:g.178530626C>A	GRCh38
NC_000002.11:g.179395353C>A , CM000664.1:g.179395353C>A	GRCh37
NC_000002.10:g.179103599C>A	NCBI36
NG_011618.3:g.305177G>T , LRG_391:g.305177G>T
NG_051363.1:g.12800C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98285G>T (TTN)	ENSP00000343764.6:p.Gly32762Val
ENST00000342175.11:c.79370G>T (TTN)	ENSP00000340554.6:p.Gly26457Val
ENST00000359218.10:c.79169G>T (TTN)	ENSP00000352154.5:p.Gly26390Val
ENST00000342175.10:c.79370G>T (TTN)	ENSP00000340554.6:p.Gly26457Val
ENST00000342992.10:c.98285G>T (TTN)	ENSP00000343764.6:p.Gly32762Val
ENST00000359218.9:c.79169G>T (TTN)	ENSP00000352154.5:p.Gly26390Val
ENST00000460472.6:c.78794G>T (TTN)	ENSP00000434586.1:p.Gly26265Val
ENST00000589042.5:c.105989G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly35330Val
ENST00000591111.5:c.101066G>T (TTN)	ENSP00000465570.1:p.Gly33689Val
ENST00000615779.4:c.101066G>T (TTN)	ENSP00000483597.1:p.Gly33689Val
NM_001256850.1:c.101066G>T (TTN)	NP_001243779.1:p.Gly33689Val
NM_001267550.2:c.105989G>T (TTN) MANE Select	NP_001254479.2:p.Gly35330Val
NM_003319.4:c.78794G>T (TTN)	NP_003310.4:p.Gly26265Val
NM_133378.4:c.98285G>T (TTN)	NP_596869.4:p.Gly32762Val
NM_133432.3:c.79169G>T (TTN)	NP_597676.3:p.Gly26390Val
NM_133437.4:c.79370G>T (TTN)	NP_597681.4:p.Gly26457Val
NR_038271.1:n.446+6990C>A (TTN-AS1)
NR_038272.1:n.220-5106C>A (TTN-AS1)
XM_011511729.1:c.105086G>T (TTN)	XP_011510031.1:p.Gly35029Val
XM_011511730.1:c.78980G>T (TTN)	XP_011510032.1:p.Gly26327Val
XM_011511731.1:c.78839G>T (TTN)	XP_011510033.1:p.Gly26280Val
XM_017004819.1:c.104882G>T (TTN)	XP_016860308.1:p.Gly34961Val
XM_017004820.1:c.100280G>T (TTN)	XP_016860309.1:p.Gly33427Val
XM_017004821.1:c.100277G>T (TTN)	XP_016860310.1:p.Gly33426Val
XM_017004822.1:c.97319G>T (TTN)	XP_016860311.1:p.Gly32440Val
XM_017004823.1:c.78935G>T (TTN)	XP_016860312.1:p.Gly26312Val
XM_024453094.1:c.100430G>T (TTN)	XP_024308862.1:p.Gly33477Val
XM_024453095.1:c.100427G>T (TTN)	XP_024308863.1:p.Gly33476Val
XM_024453096.1:c.99860G>T (TTN)	XP_024308864.1:p.Gly33287Val
XM_024453097.1:c.97202G>T (TTN)	XP_024308865.1:p.Gly32401Val
XM_024453098.1:c.97121G>T (TTN)	XP_024308866.1:p.Gly32374Val
XM_024453099.1:c.78884G>T (TTN)	XP_024308867.1:p.Gly26295Val
XM_024453100.1:c.68738G>T (TTN)	XP_024308868.1:p.Gly22913Val