Canonical Allele Identifier: CA1310521198

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543930C= , CM000664.2:g.178543930C=	GRCh38
NC_000002.11:g.179408657C= , CM000664.1:g.179408657C=	GRCh37
NC_000002.10:g.179116903C=	NCBI36
NG_011618.3:g.291873G= , LRG_391:g.291873G=
NG_051363.1:g.26104C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88510G= (TTN)	ENSP00000343764.6:p.Val29504=
ENST00000342175.11:c.69595G= (TTN)	ENSP00000340554.6:p.Val23199=
ENST00000359218.10:c.69394G= (TTN)	ENSP00000352154.5:p.Val23132=
ENST00000342175.10:c.69595G= (TTN)	ENSP00000340554.6:p.Val23199=
ENST00000342992.10:c.88510G= (TTN)	ENSP00000343764.6:p.Val29504=
ENST00000359218.9:c.69394G= (TTN)	ENSP00000352154.5:p.Val23132=
ENST00000460472.6:c.69019G= (TTN)	ENSP00000434586.1:p.Val23007=
ENST00000589042.5:c.96214G= (TTN) MANE Select	ENSP00000467141.1:p.Val32072=
ENST00000591111.5:c.91291G= (TTN)	ENSP00000465570.1:p.Val30431=
ENST00000615779.4:c.91291G= (TTN)	ENSP00000483597.1:p.Val30431=
NM_001256850.1:c.91291G= (TTN)	NP_001243779.1:p.Val30431=
NM_001267550.2:c.96214G= (TTN) MANE Select	NP_001254479.2:p.Val32072=
NM_003319.4:c.69019G= (TTN)	NP_003310.4:p.Val23007=
NM_133378.4:c.88510G= (TTN)	NP_596869.4:p.Val29504=
NM_133432.3:c.69394G= (TTN)	NP_597676.3:p.Val23132=
NM_133437.4:c.69595G= (TTN)	NP_597681.4:p.Val23199=
NR_038271.1:n.446+20294C= (TTN-AS1)
NR_038272.1:n.2043+1569C= (TTN-AS1)
XM_011511729.1:c.95311G= (TTN)	XP_011510031.1:p.Val31771=
XM_011511730.1:c.69205G= (TTN)	XP_011510032.1:p.Val23069=
XM_011511731.1:c.69064G= (TTN)	XP_011510033.1:p.Val23022=
XM_017004819.1:c.95107G= (TTN)	XP_016860308.1:p.Val31703=
XM_017004820.1:c.90505G= (TTN)	XP_016860309.1:p.Val30169=
XM_017004821.1:c.90502G= (TTN)	XP_016860310.1:p.Val30168=
XM_017004822.1:c.87544G= (TTN)	XP_016860311.1:p.Val29182=
XM_017004823.1:c.69160G= (TTN)	XP_016860312.1:p.Val23054=
XM_024453094.1:c.90655G= (TTN)	XP_024308862.1:p.Val30219=
XM_024453095.1:c.90652G= (TTN)	XP_024308863.1:p.Val30218=
XM_024453096.1:c.90085G= (TTN)	XP_024308864.1:p.Val30029=
XM_024453097.1:c.87427G= (TTN)	XP_024308865.1:p.Val29143=
XM_024453098.1:c.87346G= (TTN)	XP_024308866.1:p.Val29116=
XM_024453099.1:c.69109G= (TTN)	XP_024308867.1:p.Val23037=
XM_024453100.1:c.58963G= (TTN)	XP_024308868.1:p.Val19655=