Canonical Allele Identifier: CA349523971

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178675037A>G , CM000664.2:g.178675037A>G	GRCh38
NC_000002.11:g.179539764A>G , CM000664.1:g.179539764A>G	GRCh37
NC_000002.10:g.179248009A>G	NCBI36
NG_011618.3:g.160766T>C , LRG_391:g.160766T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.34612+2T>C MANE Select	NP_001254479.2:n.34612+2T>C
ENST00000589042.5:c.34612+2T>C MANE Select	ENSP00000467141.1:n.34612+2T>C
NM_001256850.1:c.33490+2T>C	NP_001243779.1:n.33490+2T>C
NM_003319.4:c.13283-32720T>C	NP_003310.4:n.13283-32720T>C
NM_133378.4:c.30709+2T>C	NP_596869.4:n.30709+2T>C
NM_133432.3:c.13658-32720T>C	NP_597676.3:n.13658-32720T>C
NM_133437.4:c.13859-32720T>C	NP_597681.4:n.13859-32720T>C
ENST00000342175.10:c.13859-32720T>C	ENSP00000340554.6:n.13859-32720T>C
ENST00000342175.11:c.13859-32720T>C	ENSP00000340554.6:n.13859-32720T>C
ENST00000342992.10:c.30709+2T>C	ENSP00000343764.6:n.30709+2T>C
ENST00000342992.11:c.30709+2T>C	ENSP00000343764.6:n.30709+2T>C
ENST00000359218.10:c.13658-32720T>C	ENSP00000352154.5:n.13658-32720T>C
ENST00000359218.9:c.13658-32720T>C	ENSP00000352154.5:n.13658-32720T>C
ENST00000414766.5:c.2267-628T>C	ENSP00000401501.1:n.2267-628T>C
ENST00000460472.6:c.13283-32720T>C	ENSP00000434586.1:n.13283-32720T>C
ENST00000591111.5:c.33490+2T>C	ENSP00000465570.1:n.33490+2T>C
ENST00000615779.4:c.33490+2T>C	ENSP00000483597.1:n.33490+2T>C
XM_011511729.1:c.33709+2T>C	XP_011510031.1:n.33709+2T>C
XM_011511730.1:c.13469-32720T>C	XP_011510032.1:n.13469-32720T>C
XM_011511731.1:c.13328-32720T>C	XP_011510033.1:n.13328-32720T>C
XM_017004819.1:c.33664+2T>C	XP_016860308.1:n.33664+2T>C
XM_017004820.1:c.30712+2T>C	XP_016860309.1:n.30712+2T>C
XM_017004821.1:c.30709+2T>C	XP_016860310.1:n.30709+2T>C
XM_017004822.1:c.31685-628T>C	XP_016860311.1:n.31685-628T>C
XM_017004823.1:c.13424-32720T>C	XP_016860312.1:n.13424-32720T>C
XM_024453094.1:c.33047-628T>C	XP_024308862.1:n.33047-628T>C
XM_024453095.1:c.33121+2T>C	XP_024308863.1:n.33121+2T>C
XM_024453096.1:c.32477-628T>C	XP_024308864.1:n.32477-628T>C
XM_024453097.1:c.31517-628T>C	XP_024308865.1:n.31517-628T>C
XM_024453098.1:c.31436-628T>C	XP_024308866.1:n.31436-628T>C
XM_024453099.1:c.13424-32720T>C	XP_024308867.1:n.13424-32720T>C