Canonical Allele Identifier: CA349635752

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179486379C>G (hg19) ; chr2:g.178621652C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621652C>G , CM000664.2:g.178621652C>G	GRCh38
NC_000002.11:g.179486379C>G , CM000664.1:g.179486379C>G	GRCh37
NC_000002.10:g.179194624C>G	NCBI36
NG_011618.3:g.214151G>C , LRG_391:g.214151G>C
NG_051363.1:g.103826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37468G>C	ENSP00000343764.6:p.Gly12490Arg
ENST00000342175.11:c.18553G>C	ENSP00000340554.6:p.Gly6185Arg
ENST00000359218.10:c.18352G>C	ENSP00000352154.5:p.Gly6118Arg
ENST00000342175.10:c.18553G>C	ENSP00000340554.6:p.Gly6185Arg
ENST00000342992.10:c.37468G>C	ENSP00000343764.6:p.Gly12490Arg
ENST00000359218.9:c.18352G>C	ENSP00000352154.5:p.Gly6118Arg
ENST00000460472.6:c.17977G>C	ENSP00000434586.1:p.Gly5993Arg
ENST00000589042.5:c.45172G>C MANE Select	ENSP00000467141.1:p.Gly15058Arg
ENST00000591111.5:c.40249G>C	ENSP00000465570.1:p.Gly13417Arg
ENST00000615779.4:c.40249G>C	ENSP00000483597.1:p.Gly13417Arg
NM_001256850.1:c.40249G>C	NP_001243779.1:p.Gly13417Arg
NM_001267550.2:c.45172G>C MANE Select	NP_001254479.2:p.Gly15058Arg
NM_003319.4:c.17977G>C	NP_003310.4:p.Gly5993Arg
NM_133378.4:c.37468G>C	NP_596869.4:p.Gly12490Arg
NM_133432.3:c.18352G>C	NP_597676.3:p.Gly6118Arg
NM_133437.4:c.18553G>C	NP_597681.4:p.Gly6185Arg
XM_011511729.1:c.44269G>C	XP_011510031.1:p.Gly14757Arg
XM_011511730.1:c.18163G>C	XP_011510032.1:p.Gly6055Arg
XM_011511731.1:c.18022G>C	XP_011510033.1:p.Gly6008Arg
XM_017004819.1:c.44065G>C	XP_016860308.1:p.Gly14689Arg
XM_017004820.1:c.39463G>C	XP_016860309.1:p.Gly13155Arg
XM_017004821.1:c.39460G>C	XP_016860310.1:p.Gly13154Arg
XM_017004822.1:c.36502G>C	XP_016860311.1:p.Gly12168Arg
XM_017004823.1:c.18118G>C	XP_016860312.1:p.Gly6040Arg
XM_024453094.1:c.39613G>C	XP_024308862.1:p.Gly13205Arg
XM_024453095.1:c.39610G>C	XP_024308863.1:p.Gly13204Arg
XM_024453096.1:c.39043G>C	XP_024308864.1:p.Gly13015Arg
XM_024453097.1:c.36385G>C	XP_024308865.1:p.Gly12129Arg
XM_024453098.1:c.36304G>C	XP_024308866.1:p.Gly12102Arg
XM_024453099.1:c.18067G>C	XP_024308867.1:p.Gly6023Arg
XM_024453100.1:c.7921G>C	XP_024308868.1:p.Gly2641Arg