Canonical Allele Identifier: CA1310521526

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544345T= , CM000664.2:g.178544345T=	GRCh38
NC_000002.11:g.179409072T= , CM000664.1:g.179409072T=	GRCh37
NC_000002.10:g.179117318T=	NCBI36
NG_011618.3:g.291458A= , LRG_391:g.291458A=
NG_051363.1:g.26519T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88180A= (TTN)	ENSP00000343764.6:p.Asn29394=
ENST00000342175.11:c.69265A= (TTN)	ENSP00000340554.6:p.Asn23089=
ENST00000359218.10:c.69064A= (TTN)	ENSP00000352154.5:p.Asn23022=
ENST00000342175.10:c.69265A= (TTN)	ENSP00000340554.6:p.Asn23089=
ENST00000342992.10:c.88180A= (TTN)	ENSP00000343764.6:p.Asn29394=
ENST00000359218.9:c.69064A= (TTN)	ENSP00000352154.5:p.Asn23022=
ENST00000460472.6:c.68689A= (TTN)	ENSP00000434586.1:p.Asn22897=
ENST00000589042.5:c.95884A= (TTN) MANE Select	ENSP00000467141.1:p.Asn31962=
ENST00000591111.5:c.90961A= (TTN)	ENSP00000465570.1:p.Asn30321=
ENST00000615779.4:c.90961A= (TTN)	ENSP00000483597.1:p.Asn30321=
NM_001256850.1:c.90961A= (TTN)	NP_001243779.1:p.Asn30321=
NM_001267550.2:c.95884A= (TTN) MANE Select	NP_001254479.2:p.Asn31962=
NM_003319.4:c.68689A= (TTN)	NP_003310.4:p.Asn22897=
NM_133378.4:c.88180A= (TTN)	NP_596869.4:p.Asn29394=
NM_133432.3:c.69064A= (TTN)	NP_597676.3:p.Asn23022=
NM_133437.4:c.69265A= (TTN)	NP_597681.4:p.Asn23089=
NR_038271.1:n.446+20709T= (TTN-AS1)
NR_038272.1:n.2043+1984T= (TTN-AS1)
XM_011511729.1:c.94981A= (TTN)	XP_011510031.1:p.Asn31661=
XM_011511730.1:c.68875A= (TTN)	XP_011510032.1:p.Asn22959=
XM_011511731.1:c.68734A= (TTN)	XP_011510033.1:p.Asn22912=
XM_017004819.1:c.94777A= (TTN)	XP_016860308.1:p.Asn31593=
XM_017004820.1:c.90175A= (TTN)	XP_016860309.1:p.Asn30059=
XM_017004821.1:c.90172A= (TTN)	XP_016860310.1:p.Asn30058=
XM_017004822.1:c.87214A= (TTN)	XP_016860311.1:p.Asn29072=
XM_017004823.1:c.68830A= (TTN)	XP_016860312.1:p.Asn22944=
XM_024453094.1:c.90325A= (TTN)	XP_024308862.1:p.Asn30109=
XM_024453095.1:c.90322A= (TTN)	XP_024308863.1:p.Asn30108=
XM_024453096.1:c.89755A= (TTN)	XP_024308864.1:p.Asn29919=
XM_024453097.1:c.87097A= (TTN)	XP_024308865.1:p.Asn29033=
XM_024453098.1:c.87016A= (TTN)	XP_024308866.1:p.Asn29006=
XM_024453099.1:c.68779A= (TTN)	XP_024308867.1:p.Asn22927=
XM_024453100.1:c.58633A= (TTN)	XP_024308868.1:p.Asn19545=