Canonical Allele Identifier: CA349652144

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179497710C>A (hg19) ; chr2:g.178632983C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178632983C>A , CM000664.2:g.178632983C>A	GRCh38
NC_000002.11:g.179497710C>A , CM000664.1:g.179497710C>A	GRCh37
NC_000002.10:g.179205955C>A	NCBI36
NG_011618.3:g.202820G>T , LRG_391:g.202820G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.35444G>T	ENSP00000343764.6:p.Gly11815Val
ENST00000342175.11:c.16529G>T	ENSP00000340554.6:p.Gly5510Val
ENST00000359218.10:c.16328G>T	ENSP00000352154.5:p.Gly5443Val
ENST00000342175.10:c.16529G>T	ENSP00000340554.6:p.Gly5510Val
ENST00000342992.10:c.35444G>T	ENSP00000343764.6:p.Gly11815Val
ENST00000359218.9:c.16328G>T	ENSP00000352154.5:p.Gly5443Val
ENST00000460472.6:c.15953G>T	ENSP00000434586.1:p.Gly5318Val
ENST00000589042.5:c.43148G>T MANE Select	ENSP00000467141.1:p.Gly14383Val
ENST00000591111.5:c.38225G>T	ENSP00000465570.1:p.Gly12742Val
ENST00000615779.4:c.38225G>T	ENSP00000483597.1:p.Gly12742Val
NM_001256850.1:c.38225G>T	NP_001243779.1:p.Gly12742Val
NM_001267550.2:c.43148G>T MANE Select	NP_001254479.2:p.Gly14383Val
NM_003319.4:c.15953G>T	NP_003310.4:p.Gly5318Val
NM_133378.4:c.35444G>T	NP_596869.4:p.Gly11815Val
NM_133432.3:c.16328G>T	NP_597676.3:p.Gly5443Val
NM_133437.4:c.16529G>T	NP_597681.4:p.Gly5510Val
XM_011511729.1:c.42245G>T	XP_011510031.1:p.Gly14082Val
XM_011511730.1:c.16139G>T	XP_011510032.1:p.Gly5380Val
XM_011511731.1:c.15998G>T	XP_011510033.1:p.Gly5333Val
XM_017004819.1:c.42041G>T	XP_016860308.1:p.Gly14014Val
XM_017004820.1:c.37439G>T	XP_016860309.1:p.Gly12480Val
XM_017004821.1:c.37436G>T	XP_016860310.1:p.Gly12479Val
XM_017004822.1:c.34478G>T	XP_016860311.1:p.Gly11493Val
XM_017004823.1:c.16094G>T	XP_016860312.1:p.Gly5365Val
XM_024453094.1:c.37589G>T	XP_024308862.1:p.Gly12530Val
XM_024453095.1:c.37586G>T	XP_024308863.1:p.Gly12529Val
XM_024453096.1:c.37019G>T	XP_024308864.1:p.Gly12340Val
XM_024453097.1:c.34361G>T	XP_024308865.1:p.Gly11454Val
XM_024453098.1:c.34280G>T	XP_024308866.1:p.Gly11427Val
XM_024453099.1:c.16043G>T	XP_024308867.1:p.Gly5348Val
XM_024453100.1:c.5897G>T	XP_024308868.1:p.Gly1966Val