Canonical Allele Identifier: CA1310521186

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543916A= , CM000664.2:g.178543916A=	GRCh38
NC_000002.11:g.179408643A= , CM000664.1:g.179408643A=	GRCh37
NC_000002.10:g.179116889A=	NCBI36
NG_011618.3:g.291887T= , LRG_391:g.291887T=
NG_051363.1:g.26090A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88524T= (TTN)	ENSP00000343764.6:p.Asn29508=
ENST00000342175.11:c.69609T= (TTN)	ENSP00000340554.6:p.Asn23203=
ENST00000359218.10:c.69408T= (TTN)	ENSP00000352154.5:p.Asn23136=
ENST00000342175.10:c.69609T= (TTN)	ENSP00000340554.6:p.Asn23203=
ENST00000342992.10:c.88524T= (TTN)	ENSP00000343764.6:p.Asn29508=
ENST00000359218.9:c.69408T= (TTN)	ENSP00000352154.5:p.Asn23136=
ENST00000460472.6:c.69033T= (TTN)	ENSP00000434586.1:p.Asn23011=
ENST00000589042.5:c.96228T= (TTN) MANE Select	ENSP00000467141.1:p.Asn32076=
ENST00000591111.5:c.91305T= (TTN)	ENSP00000465570.1:p.Asn30435=
ENST00000615779.4:c.91305T= (TTN)	ENSP00000483597.1:p.Asn30435=
NM_001256850.1:c.91305T= (TTN)	NP_001243779.1:p.Asn30435=
NM_001267550.2:c.96228T= (TTN) MANE Select	NP_001254479.2:p.Asn32076=
NM_003319.4:c.69033T= (TTN)	NP_003310.4:p.Asn23011=
NM_133378.4:c.88524T= (TTN)	NP_596869.4:p.Asn29508=
NM_133432.3:c.69408T= (TTN)	NP_597676.3:p.Asn23136=
NM_133437.4:c.69609T= (TTN)	NP_597681.4:p.Asn23203=
NR_038271.1:n.446+20280A= (TTN-AS1)
NR_038272.1:n.2043+1555A= (TTN-AS1)
XM_011511729.1:c.95325T= (TTN)	XP_011510031.1:p.Asn31775=
XM_011511730.1:c.69219T= (TTN)	XP_011510032.1:p.Asn23073=
XM_011511731.1:c.69078T= (TTN)	XP_011510033.1:p.Asn23026=
XM_017004819.1:c.95121T= (TTN)	XP_016860308.1:p.Asn31707=
XM_017004820.1:c.90519T= (TTN)	XP_016860309.1:p.Asn30173=
XM_017004821.1:c.90516T= (TTN)	XP_016860310.1:p.Asn30172=
XM_017004822.1:c.87558T= (TTN)	XP_016860311.1:p.Asn29186=
XM_017004823.1:c.69174T= (TTN)	XP_016860312.1:p.Asn23058=
XM_024453094.1:c.90669T= (TTN)	XP_024308862.1:p.Asn30223=
XM_024453095.1:c.90666T= (TTN)	XP_024308863.1:p.Asn30222=
XM_024453096.1:c.90099T= (TTN)	XP_024308864.1:p.Asn30033=
XM_024453097.1:c.87441T= (TTN)	XP_024308865.1:p.Asn29147=
XM_024453098.1:c.87360T= (TTN)	XP_024308866.1:p.Asn29120=
XM_024453099.1:c.69123T= (TTN)	XP_024308867.1:p.Asn23041=
XM_024453100.1:c.58977T= (TTN)	XP_024308868.1:p.Asn19659=