Canonical Allele Identifier: CA349635746

Gene: TTN

Linked Data

• dbSNP Id: rs2058298733
• MyVariant Identifiers: chr2:g.179486378C>T (hg19) ; chr2:g.178621651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621651C>T , CM000664.2:g.178621651C>T	GRCh38
NC_000002.11:g.179486378C>T , CM000664.1:g.179486378C>T	GRCh37
NC_000002.10:g.179194623C>T	NCBI36
NG_011618.3:g.214152G>A , LRG_391:g.214152G>A
NG_051363.1:g.103825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37469G>A	ENSP00000343764.6:p.Gly12490Asp
ENST00000342175.11:c.18554G>A	ENSP00000340554.6:p.Gly6185Asp
ENST00000359218.10:c.18353G>A	ENSP00000352154.5:p.Gly6118Asp
ENST00000342175.10:c.18554G>A	ENSP00000340554.6:p.Gly6185Asp
ENST00000342992.10:c.37469G>A	ENSP00000343764.6:p.Gly12490Asp
ENST00000359218.9:c.18353G>A	ENSP00000352154.5:p.Gly6118Asp
ENST00000460472.6:c.17978G>A	ENSP00000434586.1:p.Gly5993Asp
ENST00000589042.5:c.45173G>A MANE Select	ENSP00000467141.1:p.Gly15058Asp
ENST00000591111.5:c.40250G>A	ENSP00000465570.1:p.Gly13417Asp
ENST00000615779.4:c.40250G>A	ENSP00000483597.1:p.Gly13417Asp
NM_001256850.1:c.40250G>A	NP_001243779.1:p.Gly13417Asp
NM_001267550.2:c.45173G>A MANE Select	NP_001254479.2:p.Gly15058Asp
NM_003319.4:c.17978G>A	NP_003310.4:p.Gly5993Asp
NM_133378.4:c.37469G>A	NP_596869.4:p.Gly12490Asp
NM_133432.3:c.18353G>A	NP_597676.3:p.Gly6118Asp
NM_133437.4:c.18554G>A	NP_597681.4:p.Gly6185Asp
XM_011511729.1:c.44270G>A	XP_011510031.1:p.Gly14757Asp
XM_011511730.1:c.18164G>A	XP_011510032.1:p.Gly6055Asp
XM_011511731.1:c.18023G>A	XP_011510033.1:p.Gly6008Asp
XM_017004819.1:c.44066G>A	XP_016860308.1:p.Gly14689Asp
XM_017004820.1:c.39464G>A	XP_016860309.1:p.Gly13155Asp
XM_017004821.1:c.39461G>A	XP_016860310.1:p.Gly13154Asp
XM_017004822.1:c.36503G>A	XP_016860311.1:p.Gly12168Asp
XM_017004823.1:c.18119G>A	XP_016860312.1:p.Gly6040Asp
XM_024453094.1:c.39614G>A	XP_024308862.1:p.Gly13205Asp
XM_024453095.1:c.39611G>A	XP_024308863.1:p.Gly13204Asp
XM_024453096.1:c.39044G>A	XP_024308864.1:p.Gly13015Asp
XM_024453097.1:c.36386G>A	XP_024308865.1:p.Gly12129Asp
XM_024453098.1:c.36305G>A	XP_024308866.1:p.Gly12102Asp
XM_024453099.1:c.18068G>A	XP_024308867.1:p.Gly6023Asp
XM_024453100.1:c.7922G>A	XP_024308868.1:p.Gly2641Asp