Canonical Allele Identifier: CA349635748

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179486378C>A (hg19) ; chr2:g.178621651C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37469G>T	ENSP00000343764.6:p.Gly12490Val
ENST00000342175.11:c.18554G>T	ENSP00000340554.6:p.Gly6185Val
ENST00000359218.10:c.18353G>T	ENSP00000352154.5:p.Gly6118Val
ENST00000342175.10:c.18554G>T	ENSP00000340554.6:p.Gly6185Val
ENST00000342992.10:c.37469G>T	ENSP00000343764.6:p.Gly12490Val
ENST00000359218.9:c.18353G>T	ENSP00000352154.5:p.Gly6118Val
ENST00000460472.6:c.17978G>T	ENSP00000434586.1:p.Gly5993Val
ENST00000589042.5:c.45173G>T MANE Select	ENSP00000467141.1:p.Gly15058Val
ENST00000591111.5:c.40250G>T	ENSP00000465570.1:p.Gly13417Val
ENST00000615779.4:c.40250G>T	ENSP00000483597.1:p.Gly13417Val
NM_001256850.1:c.40250G>T	NP_001243779.1:p.Gly13417Val
NM_001267550.2:c.45173G>T MANE Select	NP_001254479.2:p.Gly15058Val
NM_003319.4:c.17978G>T	NP_003310.4:p.Gly5993Val
NM_133378.4:c.37469G>T	NP_596869.4:p.Gly12490Val
NM_133432.3:c.18353G>T	NP_597676.3:p.Gly6118Val
NM_133437.4:c.18554G>T	NP_597681.4:p.Gly6185Val
XM_011511729.1:c.44270G>T	XP_011510031.1:p.Gly14757Val
XM_011511730.1:c.18164G>T	XP_011510032.1:p.Gly6055Val
XM_011511731.1:c.18023G>T	XP_011510033.1:p.Gly6008Val
XM_017004819.1:c.44066G>T	XP_016860308.1:p.Gly14689Val
XM_017004820.1:c.39464G>T	XP_016860309.1:p.Gly13155Val
XM_017004821.1:c.39461G>T	XP_016860310.1:p.Gly13154Val
XM_017004822.1:c.36503G>T	XP_016860311.1:p.Gly12168Val
XM_017004823.1:c.18119G>T	XP_016860312.1:p.Gly6040Val
XM_024453094.1:c.39614G>T	XP_024308862.1:p.Gly13205Val
XM_024453095.1:c.39611G>T	XP_024308863.1:p.Gly13204Val
XM_024453096.1:c.39044G>T	XP_024308864.1:p.Gly13015Val
XM_024453097.1:c.36386G>T	XP_024308865.1:p.Gly12129Val
XM_024453098.1:c.36305G>T	XP_024308866.1:p.Gly12102Val
XM_024453099.1:c.18068G>T	XP_024308867.1:p.Gly6023Val
XM_024453100.1:c.7922G>T	XP_024308868.1:p.Gly2641Val