Canonical Allele Identifier: CA60950133

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178528570G>C , CM000664.2:g.178528570G>C	GRCh38
NC_000002.11:g.179393297G>C , CM000664.1:g.179393297G>C	GRCh37
NC_000002.10:g.179101543G>C	NCBI36
NG_011618.3:g.307233C>G , LRG_391:g.307233C>G
NG_051363.1:g.10744G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107181C>G (TTN) MANE Select	NP_001254479.2:p.Gly35727=
ENST00000589042.5:c.107181C>G (TTN) MANE Select	ENSP00000467141.1:p.Gly35727=
NM_001256850.1:c.102258C>G (TTN)	NP_001243779.1:p.Gly34086=
NM_003319.4:c.79986C>G (TTN)	NP_003310.4:p.Gly26662=
NM_133378.4:c.99477C>G (TTN)	NP_596869.4:p.Gly33159=
NM_133432.3:c.80361C>G (TTN)	NP_597676.3:p.Gly26787=
NM_133437.4:c.80562C>G (TTN)	NP_597681.4:p.Gly26854=
NR_038271.1:n.446+4934G>C (TTN-AS1)
NR_038272.1:n.219+4934G>C (TTN-AS1)
ENST00000342175.10:c.80562C>G (TTN)	ENSP00000340554.6:p.Gly26854=
ENST00000342175.11:c.80562C>G (TTN)	ENSP00000340554.6:p.Gly26854=
ENST00000342992.10:c.99477C>G (TTN)	ENSP00000343764.6:p.Gly33159=
ENST00000342992.11:c.99477C>G (TTN)	ENSP00000343764.6:p.Gly33159=
ENST00000359218.10:c.80361C>G (TTN)	ENSP00000352154.5:p.Gly26787=
ENST00000359218.9:c.80361C>G (TTN)	ENSP00000352154.5:p.Gly26787=
ENST00000460472.6:c.79986C>G (TTN)	ENSP00000434586.1:p.Gly26662=
ENST00000591111.5:c.102258C>G (TTN)	ENSP00000465570.1:p.Gly34086=
ENST00000615779.4:c.102258C>G (TTN)	ENSP00000483597.1:p.Gly34086=
XM_011511729.1:c.106278C>G (TTN)	XP_011510031.1:p.Gly35426=
XM_011511730.1:c.80172C>G (TTN)	XP_011510032.1:p.Gly26724=
XM_011511731.1:c.80031C>G (TTN)	XP_011510033.1:p.Gly26677=
XM_017004819.1:c.106074C>G (TTN)	XP_016860308.1:p.Gly35358=
XM_017004820.1:c.101472C>G (TTN)	XP_016860309.1:p.Gly33824=
XM_017004821.1:c.101469C>G (TTN)	XP_016860310.1:p.Gly33823=
XM_017004822.1:c.98511C>G (TTN)	XP_016860311.1:p.Gly32837=
XM_017004823.1:c.80127C>G (TTN)	XP_016860312.1:p.Gly26709=
XM_024453094.1:c.101622C>G (TTN)	XP_024308862.1:p.Gly33874=
XM_024453095.1:c.101619C>G (TTN)	XP_024308863.1:p.Gly33873=
XM_024453096.1:c.101052C>G (TTN)	XP_024308864.1:p.Gly33684=
XM_024453097.1:c.98394C>G (TTN)	XP_024308865.1:p.Gly32798=
XM_024453098.1:c.98313C>G (TTN)	XP_024308866.1:p.Gly32771=
XM_024453099.1:c.80076C>G (TTN)	XP_024308867.1:p.Gly26692=
XM_024453100.1:c.69930C>G (TTN)	XP_024308868.1:p.Gly23310=